Albadry Plus: Product Information

ALBADRY PLUS- novobiocin sodium and penicillin g procaine injection, solution
Zoetis Inc.

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)in a special bland vehicle 50 mg

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

  • Do not use less than 30 days prior to calving.
  • Milk from treated cows must not be used for food during the first 72 hours after calving.
  • Treated animals must not be slaughtered for food for 30 days following udder infusion.

PRECAUTION

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 ⅛ inch of the cannula, as recommended by the National Mastitis Council.

  • Full Insertion: Remove the blue end cap by pulling straight up as shown. Gently insert the full cannula into the teat canal; carefully infuse the product.
    • Figure a.
  • Partial Insertion: Remove both the blue end cap and the red cannula by pushing sideways as shown. Gently insert the exposed blue tip into the teat canal; carefully infuse the product.
    • Figure b.
Figure a.Figure b.

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 REUSE KEEP OUT OF REACH OF CHILDREN

STORAGE CONDITIONS

Store at controlled room temperature 20° to 25° C (68° to 77° F).

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.

Approved by FDA under NADA #055-098

Product of the United Kingdom
Zoetis Inc.
Kalamazoo, MI 49007 USA
By Norbrook Laboratories Limited
Newry, BT35 6JP, Northern Ireland
Revised: April 2020

002544L09

PRINCIPAL DISPLAY PANEL — 10 mL Syringe Label

10 mL (.33 FI Oz) Suspension

ALBADRY PLUS® Suspension

penicillin G procaine and novobiocin sodium intramammary infusion

DRY COW FORMULA

PRINCIPAL DISPLAY PANEL -- 10 mL Syringe Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 12 x 10 mL Syringe Carton

ALBADRY PLUS®
Suspension

PENICILLIN G PROCAINE AND NOVOBIOCIN SODIUM INTRAMAMMARY INFUSION

DRY COW FORMULA

Indicated for intramammary infusion in the treatment of subclinical mastitis caused by
susceptible strains of Staphylococcus aureus and Streptococcus agalactiae.

Contains: 400 mg novobiocin sodium plus 200,000 IU penicillin G procaine
per 10 mL syringe

Approved by FDA under NADA #055-098 12-10 mL (.33 FI Oz) PLASTET® Disposable Syringes / 12 ALCOHOL PADS INCLUDED

zoetis

Albadry Plus Suspension Carton
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 144 x 10 mL Syringe Pail Label

TAKE TIME
OBSERVE LABEL
DIRECTIONS

ALBADRY PLUS®
Suspension

PENICILLIN G PROCAINE AND NOVOBIOCIN SODIUM

DRY COW FORMULA

Indicated for intramammary infusion in the treatment of subclinical mastitis caused by
susceptible strains of Staphylococcus aureus and Streptococcus agalactiae.

Contains: 400 mg novobiocin sodium plus 200,000 IU penicillin G procaine
per 10 mL syringe

1404000
002544L04

Approved by FDA under NADA #055-098144-10 mL (.33 FI Oz) PLASTET® Disposable Syringes / 144 ALCOHOL PADS INCLUDED

zoetis

Albadry Plus Suspension Label
(click image for full-size original)
ALBADRY PLUS novobiocin sodium and penicillin g procaine injection, solution
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:54771-3139
Route of Administration INTRAMAMMARY DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NOVOBIOCIN SODIUM (NOVOBIOCIN) NOVOBIOCIN 400 mg in 10 mL
PENICILLIN G PROCAINE (PENICILLIN G) PENICILLIN G 200000 [iU] in 10 mL
Inactive Ingredients
Ingredient Name Strength
CHLOROBUTANOL 50 mg in 10 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:54771-3139-1 12 SYRINGE in 1 CARTON contains a SYRINGE (54771-3139-9)
1 NDC:54771-3139-9 10 mL in 1 SYRINGE This package is contained within the CARTON (54771-3139-1)
2 NDC:54771-3139-2 144 SYRINGE in 1 PAIL contains a SYRINGE (54771-3139-9)
2 NDC:54771-3139-9 10 mL in 1 SYRINGE This package is contained within the PAIL (54771-3139-2)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NADA NADA055098 01/07/1983
Labeler — Zoetis Inc. (828851555)

Revised: 07/2022 Zoetis Inc.

VetLabel.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by VetLabel.com. Every individual animal healthcare product label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

Our database mirrors the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. VetLabel.com provides the full animal health subset of the FDA's repository. Veterinary information provided here is not intended as a substitute for direct consultation with a qualified veterinary professional.

Terms of Use | Copyright © 2022. All Rights Reserved.