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Acetazolam N+ 500Mg Vl By X-Gen Pharmaceuticals Injectab

Item No.: RX309773 ACETAZOLAM N+ 500MG                 VL  by X-GEN PHARMACEUTICALS INJECTAB  NDC No.: 39822019007,  39822-0190-07, 39822019007, 39822-0190-07, 39822-01-9007, 39822019007 UPC No.: 3982X/Gen PharmaceuticalImage 4 of Acetazolam N+ 500Mg                 Vl  By X-Gen Pharmaceuticals Injectab

Acetazolam N+ 500Mg Vl By X-Gen Pharmaceuticals Injectab


Item No.: Rx309773 Acetazolam N+ 500Mg Vl By X-Gen Pharmaceuticals Injectab Ndc No.: 39822019007, 39822-0190-07, 39822019007, 39822-0190-07, 39822-01-9007, 39822019007 Upc No.: 39822019007' 33982201907, 39822019007, 3-39822-01907-6, 339822019076 Generic Name: Acetazolamide Sodium Inje Mfg. Name: X-Gen Pharmaceuticals Injectab, 3938000 Mpn No.; 19007 Brand: N Item Category: Rx Upc Last Check Digit: -6

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U.S. BRAND NAMES Diamox? Sequels?
Anticonvulsant, Miscellaneous
Carbonic Anhydrase Inhibitor
Diuretic, Carbonic Anhydrase Inhibitor
Ophthalmic Agent, Antiglaucoma
DOSING: ADULTS Note: I.M. administration is not recommended.
Chronic simple (open-angle): Oral: 250 mg 1-4 times/day or 500 mg extended release capsule twice daily
Secondary, acute (closed-angle): I.V.: 250-500 mg, may repeat in 2-4 hours to maximum of g/day
Edema: Oral, I.V.: 250-375 mg once daily
Epilepsy: Oral: 8-30 mg/kg/day in 1-4 divided doses, not to exceed g/day. Note: Extended release capsule is not recommended for treatment of epilepsy.
Metabolic alkalosis (unlabeled use): I.V. 250 mg every hours for doses or 500 mg single dose; reassess need based upon acid-base status
Mountain sickness: Oral: 250 mg every 8-12 hours (or 500 mg extended release capsules every 12-24 hours). Therapy should begin 24-48 hours before and continue during ascent and for at least 48 hours after arrival at the high altitude.
Note: In situations of rapid ascent (such as rescue or military operations), 1000 mg/day is recommended.
Urine alkalinization (unlabeled use): Oral: mg/kg/dose repeated 2-3 times over 24 hours
Respiratory stimulant in COPD (unlabeled use): Oral, I.V.: 250 mg twice daily
DOSING: PEDIATRIC Note: I.M. administration is not recommended.

AcetaZOLAMIDE for Injection, USP 500 mg Front Back Printing. To be supplied in folded size of 30 60 mm. Brand name facing front after final folding. 40/45 GSM Paper. Black Printing clarity to be clear sharp. NA AcetaZOLAMIDE for Injection, USP (For Intravenous Use Only) DESCRIPTION Acetazolamide, an inhibitor of the enzyme carbonic anhydrase, is white to faintly yellowish white crystalline, odorless powder, weakly acidic, very slightly soluble in water and slightly soluble in alcohol. The chemical name for acetazolamide is N-(5-Sulfamoyl- 1,3,4-thiadiazol-2yl)-acetamide and has the following chemical structure: M.W. 222.24 4 6 4 3 2 Acetazolamide is available for intravenous use, and is supplied as sterile powder requiring reconstitution. Each vial contains acetazolamide sodium equivalent to 500 mg of acetazolamide. The bulk solution is adjusted to pH 9.6 using sodium hydroxide and, if necessary, hydrochloric acid prior to lyophilization. CLINICAL PHARMACOLOGY Acetazolamide is potent carbonic anhydrase inhibitor, effective in the control of fluid secretion (e.g., some types of glaucoma), in the treatment of certain convulsive disorders (e.g., epilepsy) and in the promotion of diuresis in instances of abnormal fluid retention (e.g., cardiac edema). Acetazolamide is not mercurial diuretic. Rather, it is nonbacteriostatic sulfonamide possessing chemical structure and pharmacological activity distinctly different from the bacteriostatic sulfonamides. Acetazolamide is an enzyme inhibitor that acts specifically on carbonic anhydrase, the enzyme that catalyzes the reversible reaction involving the hydration of carbon dioxide and the dehydration of carbonic acid. In the eye, this inhibitory action of acetazolamide decreases the secretion of aqueous humor and results in drop in intraocular pressure, reaction considered desirable in cases of glaucoma and even in certain nonglaucomatous conditions. Evidence seems to indicate that acetazolamide has utility as an adjuvant in the treatment of certain dysfunctions of the central nervous system (e.g., epilepsy). Inhibition of carbonic anhydrase in this area appears to retard abnormal, paroxysmal, excessive discharge from central nervous system neurons. The diuretic effect of acetazolamide is due to its action in the kidney on the reversible reaction involving hydration of carbon dioxide and dehydration of carbonic acid. The result is renal loss of HCO ion, which carries out sodium, water, and potassium. Alkalinization of the urine and promotion of diuresis are thus effected. Alteration in ammonia metabolism occurs due to increased reabsorption of ammonia by the renal tubules as result of urinary alkalinization. INDICATIONS AND USAGE For adjunctive treatment of: edema due to congestive heart failure; drug-induced edema; centrencephalic epilepsies (petit mal, unlocalized seizures); chronic simple (open-angle) glaucoma, secondary glaucoma, and preoperatively in acute angle-closure glaucoma where delay of surgery is desired in order to lower intraocular pressure. CONTRAINDICATIONS Hypersensitivity to acetazolamide or any excipients in the formulation. Since acetazolamide is sulfonamide derivative, cross sensitivity between acetazolamide, sulfonamides and other sulfonamide derivatives is possible. Acetazolamide therapy is contraindicated in situations in which sodium and/or potassium blood serum levels are depressed, in cases of marked kidney and liver disease or dysfunction, in suprarenal gland failure, and in hyperchloremic acidosis. It is contraindicated in patients with cirrhosis because of the risk of development of hepatic encephalopathy. Long-term administration of acetazolamide is contraindicated in patients with chronic noncongestive angle-closure glaucoma since it may permit organic closure of the angle to occur while the worsening glaucoma is masked by lowered intraocular pressure. WARNINGS Fatalities have occurred, although rarely, due to severe reactions to sulfonamides including Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias. Sensitizations may recur when sulfonamide is readministered irrespective of the route of administration. If signs of hypersensitivity or other serious reactions occur, discontinue use of this drug. Caution is advised for patients receiving concomitant high-dose aspirin and acetazolamide, as anorexia, tachypnea, lethargy, coma and death have been reported. PRECAUTIONS General Increasing the dose does not increase the diuresis and may increase the incidence of drowsiness and/or paresthesia. Increasing the dose often results in decrease in diuresis. Under certain circumstances, however, very large doses have been given in conjunction with other diuretics in order to secure diuresis in complete refractory failure. info. for Patients Adverse reactions common to all sulfonamide derivatives may occur: anaphylaxis, fever, rash (including erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis), crystalluria, renal calculus, bone marrow depression, thrombocytopenic purpura, hemolytic anemia, leukopenia, pancytopenia and agranulocytosis. Precaution is advised for early detection of such reactions and the drug should be discontinued and appropriate therapy instituted. In patients with pulmonary obstruction or emphysema where alveolar ventilation may be impaired, acetazolamide which may precipitate or aggravate acidosis, should be used with caution. Caution is advised for patients receiving concomitant high-dose aspirin and acetazolamide, as anorexia, tachypnea, lethargy, coma and death have been reported (see WARNINGS ). Labora tory Tests To monitor for hematologic reactions common to all sulfonamides, it is recommended that baseline CBC and platelet count be obtained on patients prior to initiating acetazolamide therapy and at regular intervals during therapy. If significant changes occur, early discontinuance and institution of appropriate therapy are important. Periodic monitoring of serum electrolytes is recommended. Carcinogenesis, Mutagenesis, Impairment of Fertility Long-term studies in animals to evaluate the carcinogenic potential of acetazolamide have not been conducted. In bacterial mutagenicity assay, acetazolamide was not mutagenic when evaluated with and without metabolic activation. The drug had no effect on fertility when administered in the diet to male and female rats at daily intake of up to times the recommended human dose of 1000 mg in 50 kg individual. Pregnancy Teratogenic Effects: Pregnancy Category Acetazolamide, administered orally or parenterally, has been shown to be teratogenic (defects of the limbs) in mice, rats, hamsters and rabbits. There are no adequate and well-controlled studies in pregnant women. Acetazolamide should be used in pregnancy only if the potential benefit justifies the potential risk to the fetus. Nursing Mothers Because of the potential for serious adverse reaction in nursing infants from acetazolamide, decision should be made whether to discontinue nursing or to discontinue the drug taking into account the importance of the drug to the mother. Pediatric Use The safety and effectiveness of acetazolamide in children have not been established. ADVERSE REACTIONS Adverse reactions, occurring most often early in therapy, include paresthesias, particularly ?tingling? feeling in the extremities, FRONT SIDE Sagent US Pack Insert -- R1 240 120 mm 1022584 1013321 AcetaZOLAMIDE for Injection, USP 500 mg Front Back Printing. To be supplied in folded size of 30 60 mm. Brand name facing front after final folding. 40/45 GSM Paper. Black Printing clarity to be clear sharp. NA hearing dysfunction or tinn itus, loss of appetite, taste alteration and gastrointestinal disturbances such as nausea, vomiting and diarrhea; polyuria, and occasional instances of drowsiness and confusion. Metabolic acidosis and electrolyte imbalance may occur. Transient myopia has been reported. This condition invariably subsides upon diminution or discontinuance of the medication. Other occasional adverse reactions include urticaria, melena, hematuria, glycosuria, hepatic insufficiency, flaccid paralysis, photosensitivity and convulsions. Also see PRECAUTIONS: info. for Patients for possible reactions common to sulfonamide derivatives. Fatalities have occurred although rarely, due to severe reactions to sulfonamides including Stevens- Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia and other blood dyscrasias (see WARNINGS ). To report SUSPECTED ADVERSE REACTIONS, contact Sagent Pharmaceuticals, Inc. at 1-866-625-1618 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch OVERDOSAGE No data are available regarding acetazolamide overdosage in humans as no cases of acute poisoning with this drug have been reported. Animal data suggest that acetazolamide is remarkably nontoxic. No specific antidote is known. Treatment should be symptomatic and supportive. Electrolyte imbalance, development of an acidotic state, and central nervous effects might be expected to occur. Serum electrolyte levels (particularly potassium) and blood pH levels should be monitored. Supportive measures are required to restore electrolyte and pH balance. The acidotic state can usually be corrected by the administration of bicarbonate. Despite its high intraerythrocytic distribution and plasma protein binding properties, acetazolamide may be dialyzable. This may be particularly important in the management of acetazolamide overdosage when complicated by the presence of renal fa ilure. DOSAGE AND DMINISTRATION Preparation and Storage of Parenteral Solution Each 500 mg vial containing sterile acetazolamide sodium should be reconstituted with at least mL of Sterile Water for Injection prior to use. Store drug product at 20? to 25?C (68? to 77?F). [See USP Controlled Room Temperature.] Reconstituted solutions retain their physical and chemical properties for days under refrigeration at 2? 8?C (36? 46?F), or 12 hours at room temperature 20? to 25?C (68? to 77?F). CONTAINS NO PRESERVATIVE. The direct intravenous route of administration is preferred. Intramuscular administration is not recommended. Glaucoma Acetazolamide should be used as an adjunct to the usual therapy. The dosage employed in the treatment of chronic simple (open- angle) glaucoma ranges from 250 mg to g of acetazolamide per 24 hours, usually in divided doses for amounts over 250 mg. It has usually been found that dosage in excess of g per 24 hours does not produce an increased effect. In all cases, the dosage should be adjusted with careful individual attention both to symptomatology and ocular tension. Continuous supervision by physician is advisable. In treatment of secondary glaucoma and in the preoperative treatment of some cases of acute congestive (closed-angle) glaucoma, the preferred dosage is 250 mg every four hours, although some cases have responded to 250 mg twice daily on short-term therapy. In some acute cases, it may be more satisfactory to administer an initial dose of 500 mg followed by 125 or 250 mg every four hours depending on the individual case. Intravenous therapy may be used for rapid relief of ocular tension in acute cases. complementary effect has been noted when acetazolamide has been used in conjunction with miotics or mydriatics as the case demanded. Epilepsy It is not clearly known whether the beneficial effects observed in epilepsy are due to direct inhibition of carbonic anhydrase in the central nervous system or whether they are due to the slight degree of acidosis produced by the divided dosage. The best results to date have been seen in petit mal in children. Good results, however, have been seen in patients, both children and adult, in other types of seizures such as grand mal, mixed seizure patterns, myoclonic jerk patterns, etc. The suggested total daily dose is to 30 mg per kg in divided doses. Although some patients respond to low dose, the optimum range appears to be from 375 to 1000 mg daily. However, some investigators feel that daily doses in excess of g do not produce any better results than 1 dose. When acetazolamide is given in combination with other anticonvulsants, it is suggested that the starting dose should be 250 mg once daily in addition to the existing medications. This can be increased to levels as indicated above. The change from other medications to acetazolamide should be gradual and in accordance with usual practice in epilepsy therapy. Congestive Heart Failure For diuresis in congestive heart failure, the starting dose is usually 250 to 375 mg once daily in the morning (5 mg per kg). If, after an initial response, the patient fails to continue to lose edema fluid, do not increase the dose but allow for kidney recovery by skipping medication for day. Acetazolamide yields best diuretic results when given on alternate days, or for two days alternating with day of rest. Failures in therapy may be due to overdosage or too frequent dosage. The use of acetazolamide does not eliminate the need for other therapy such as digitalis, bed rest, and salt restriction. Drug-Induced Edema Recommended dosage is 250 to 375 mg of acetazolamide once day for one or two days, alternating with day of rest. Note: The dosage recommendations for glaucoma and epilepsy differ considerably from those for congestive heart failure, since the first two conditions are not dependent upon carbonic anhydrase inhibition in the kidney which requires intermittent dosage if it is to recover from inhibitory effect of the therapeutic agent. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. HOW SUPPLIED AcetaZOLAMIDE for Injection, USP (lyophilized) powder is supplied as follows: NDC AcetaZOLAMIDE Package Factor for Injection, USP 25021-817-10 500 mg Vial vial per carton Storage Conditions Store drug product at 20? to 25?C (68? to 77?F). [See USP Controlled Room Temperature.] Store reconstituted solution in refrigerator between 2? and 8?C (36? and 46?F). Use within 12 hours of reconstitution. Discard unused por tion. Sterile, Nonpyrogenic, Preservative-free. The container closure is not made with natural rubber latex. Mfd. for SAGENT Pharmaceuticals Schaumburg, IL 60195 (USA) Made in India ?2013 Sagent Pharmaceuticals, Inc. February 2013 1022584

Item No.: RX309773 ACETAZOLAM N+ 500MG                 VL  by X-GEN PHARMACEUTICALS INJECTAB  NDC No.: 39822019007,  39822-0190-07, 39822019007, 39822-0190-07, 39822-01-9007, 39822019007 UPC No.: 3982
Item No.: RX309773 ACETAZOLAM N+ 500MG VL by X-GEN PHARMACEUTICALS INJECTAB NDC No.: 39822019007, 39822-0190-07, 39822019007, 39822-0190-07, 39822-01-9007, 39822019007 UPC No.: 3982