Zoetis
NDC 0009-3139-06, NDC 0009-3139-02
brand of penicillin G procaine and novobiocin sodium suspension
For the Treatment of Subclinical Mastitis in Dry Cows
For Udder Instillation in Dry Cows Only
FOR USE IN ANIMALS ONLY - NOT FOR HUMAN USE
Restricted Drug - Use Only as Directed (California)
DESCRIPTION
Each 10 mL PLASTET® Disposable Syringe contains:
Novobiocin sodium equiv. to novobiocin
|
400 mg
|
Penicillin G procaine
|
200,000 IU
|
Chlorobutanol anhydrous (chloral derivative - used as a preservative)
|
50 mg
|
in a special bland vehicle.
Manufactured by a non-sterilizing process.
INDICATIONS FOR USE
ALBADRY PLUS Suspension is indicated for the treatment,
in dry cows only, of subclinical mastitis caused by susceptible strains
of Staphylococcus aureus and Streptococcus agalactiae.
WARNINGS
1. Do not use less than 30 days prior to calving.
2. Milk from treated cows must not be used for food during the first 72 hours after calving.
3. Treated animals must not be slaughtered for food for 30 days following udder infusion.
PRECAUTIONS
Administration of this product in any manner other than shown under DOSAGE may result in drug residues.
DOSAGE
Infuse one tube per quarter at start of dry period (but not less than 30 days prior to calving).
Shake Well Before Using
DIRECTIONS FOR USING THE FLEXI-TUBE® SYSTEM
The FLEXI-TUBE is designed to provide the choice of
either insertion of the full cannula, as has traditionally been
practiced, or insertion of no more than 1/8 inch of the cannula, as
recommended by the National Mastitis Council.
a. Full Insertion: Remove the blue
end cap by pulling straight up. Gently insert the full cannula into the
teat canal; carefully infuse the product.
b. Partial Insertion: Remove both
the blue end cap and the red cannula by pushing sideways. Gently insert
the exposed blue tip into the teat canal; carefully infuse the product.
ADMINISTRATION
At the time of drying off, but not less than 30 days
prior to calving, milk the udder dry. Wash the teats and udder
thoroughly with warm water containing a suitable dairy antiseptic. Dry
the teats and udder thoroughly. Infuse each quarter using the following
procedure. Using the alcohol pads provided, scrub each teat end clean
using a separate pad for each teat. Warm ALBADRY PLUS Suspension to body
temperature and shake thoroughly. Choose the desired insertion length
(full or partial) and insert tip into teat canal. Instill entire
contents into the quarter. Massage the udder after treatment to
distribute the ALBADRY PLUS Suspension throughout the quarters. Using a
suitable teat dip, dip all teats following treatment.
Discard Empty Container; DO NOT RE-USE
KEEP OUT OF REACH OF CHILDREN
STORAGE CONDITIONS
Store at controlled room temperature 20° to 25°C (68° to 77°F) [see USP].
HOW SUPPLIED
ALBADRY PLUS Suspension is available in unbroken
packages of 12-10 mL Plastet Disposable Syringes with 12 individually
wrapped 70% isopropyl alcohol pads and unbroken packages of 144-10 mL
Plastet Disposable Syringes with 144 individually wrapped 70% isopropyl
alcohol pads.
NADA #55-098, Approved by FDA
Made in the United Kingdom for: Pharmacia & Upjohn Company, Kalamazoo, MI 49001, U.S.A.
By Norbrook Laboratories Limited, Newry, BT35 6JP, Northern Ireland.
Revised December 1999
812 404 007
CPN: 3690467.0