V-MAX 50- virginiamycin powder

V-Max 50 by

Drug Labeling and Warnings

V-Max 50 by is a Animal medication manufactured, distributed, or labeled by Phibro Animal Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

To be mixed in cattle feed

Active Drug Ingredient

Virginiamycin : 11%

(Contains 50 g virginiamycin activity per lb)

Caution

•   CAUTION: Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

Inert ingredients :

Processed grain by-products, roughage products, calcium carbonate, carboxymethylcellulose, mineral oil

INDICATIONS & USAGE

Important: Must be diluted in feed before use

Follow Directions on Back Panel

V-Max is a registered trademark of Phibro Animal Health Corporation

Phibro Animal Health Corporation, Teaneck, NJ 07666

NADA #140-998, Approved by FDA

8812000

101-9141-05

NET CONTENTS: 50 lb (22.7 kg)

Distributed by:

PHIBRO ANIMAL HEALTH, INC.

Teaneck, NJ 07666, USA

(50 g virginiamycin activity per lb)For use in complete feeds for cattle fed in confinement for slaughter as specified belowDirections for Use

Cattle fed in confinement for slaughter	Virginiamycin required mg/hd/day	Virginiamycin (g/tons) of complete feed (90% dry matter basis)
Reduction of incidence of liver abscesse	85–240	13.5–16.0
Caution: Not for use in animals intended for breeding.

Mixing Directions

Preparation ofType B Medicated Feeds for cattle fed in confinement for slaughter—Thoroughly mix the following amounts of V-Max 50 Type A Medicated Article to make 1 ton of Type B Medicated Feed to provide the concentrations shown in Table 1. An intermediate blending step, consistent with the mixing equipment specifications, should be performed to ensure adequate mixing.

Table 1. Type B Medicated Feed

• lb of V-Max 50 Type A Medicated Article per ton of supplement:

  Virginiamycin concentration in Type B Medicated Feed (g/ton)

• 5 10 20 40 100 200:

  250

  500

  1,000

  2,000

  5,000

  10,000

Preparation of Type C Medicated Feed for cattle fed in confinement for slaughter:

From Type B Medicated Feed: The Type B Medicated Feed must be diluted to a Type C Medicated Feed before being fed. Prepare a Type B Medicated Feed as described above. Thoroughly mix the V-Max 50 Type B Medicated Feed to make 1 ton of Type C Medicated Feed to provide 13.5 16.0 g of virginiamycin per ton of complete feed on a 90% dry matter basis using the examples provided in Table 2.

Table 2. Type C Medicated Feed prepared from V-Max 50 Type B Medicated Feed

lb of a 500g/ton Type B Medicated Feed per ton of complete feed	lb of a 1,000 g/ton Type B Medicated Feed per ton of complete feed	lb of a 5,000 g/ton Type B Medicated Feed per ton of complete feed	lb of a 10,000 g/ton Type B Medicated Feed per ton of complete feed	Virginiamycin concentration in complete feed 90% dry matter basis (g/ton)
54	27	5.4	2.7	13.5
64	32	6.4	3.2	16.0

From Type A Medicated Article: V-Max 50 Type A Medicated Article must be diluted to a Type C Medicated Feed before being fed. Thoroughly mix the Type A Medicated Article to make 1 ton of Type C Medicated Feed to provide 13.5 – 16.0 g of virginiamycin per ton of complete feed on a 90% dry matter basis using the examples provided in Table 3.

An intermediate blending step, consistent with the blending equipment specifications, should be performed to ensure adequate mixing.

Table 3. Type C Medicated Feed prepared from V-Max 50 Type A Medicated Article

• lb of V-Max 50 Type A Medicated Article per ton of complete feed:

  Virginiamycin concentration in complete feed 90% dry matter basis (g/ton)

• 0.27 0.32:

  13.5

  16.0

Feed continuously as sole ration

Store at or Below 25°C/77F°, Excursions Permitted Up To 40oC (104oF)

Close container after use

INDICATIONS & USAGE

NOT FOR HUMAN USE

RESTRICTED DRUG (CALIFORNIA) – USE ONLY AS DIRECTED

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

V-MAX 50 
virginiamycin powder

Product Information
Product Type	VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG	Item Code (Source)	NDC: 66104-9601
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
VIRGINIAMYCIN (UNII: C49WS9N75L) (VIRGINIAMYCIN - UNII:C49WS9N75L)	VIRGINIAMYCIN	227 g  in 0.45 kg

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK)
MINERAL OIL (UNII: T5L8T28FGP)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66104-9601-1	22.7 kg in 1 BAG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NADA	NADA140998	04/01/2010

Labeler - Phibro Animal Health (006989008)

Registrant - Phibro Animal Health (006989008)