Vetr Ampromax (amprolium, 9.6% oral solution)

Manufacturer
Vetr LLC
Effective date
2026-05-13
Label type
OTC ANIMAL DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:47:00

Label at a glance#

ProductAmpromax
Active ingredientAMPROLIUM
Label structure6 sections

Storage and handling

Store at room temperature, at or below 25 C (

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

WARNING: NOT FOR USE IN HUMANS. Keep this and all drugs out of the reach of children. FOR ORAL USE IN ANIMALS ONLY. MAY CAUSE EYE IRRITATION. For irritation, flush with water and seek medical attention. RESUDUE WARNING: Withdraw 24 h before slaughter. A withdrawl period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

INSTRUCTIONS FOR USE SECTION

Shake well before use.

5 Day Regimen(coccidiosis symptoms present): Add Ampromax (9.6% amprolium) oral solution to drinking water at the rate of 16 fl oz/100 gal (473 mL/378.5 mL). At the usual rate of water consumption, this will provide intake of approximately 10 mg amprolium/kg body weight (2.2 lbs). Offer this solution as the only source of water for 5 days. Use on a herd basis only; when one or more calves show signs of coccidiosis, it is likely that the rest of the group has been exposed and all calves should be treated.

21 Day Regimen(coccidiosis exposure risk): During periods of exposure, or when experience indicates environmental coccidiosis risk, add Ampromax (9.6% amprolium) oral solution to drinking water at the rate of 8 fl oz/100 gal (237 mL/378.5 mL). At usual rates of consumption, this will provide approximately 5 mg amprolium/kg body weight (2.2 lbs). Offer this solution as the only source of water for 21 days.

STORAGE AND HANDLING SECTION

Store at room temperature, at or below 25 C (<77 F)

OTC - ACTIVE INGREDIENT SECTION

Amprolium USP, 96 mg/mL (9.6% w/v)

INACTIVE INGREDIENT SECTION

Purified water, preservative.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ampromax-500-labelampromax-500-label

ampromax-1gal-labelampromax-1gal-label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1092546amprolium 9.6 % Oral SolutionPSN2
2716695Ampromax 9.6 % Oral SolutionPSN2
2716695amprolium 96 MG/ML Oral Solution [Ampromax]SBD2
1092546amprolium 96 MG/ML Oral SolutionSCD2
1092546amprolium 9.6 % Oral SolutionSY2
2716695Ampromax 9.6 % Oral SolutionSY2
2716695Ampromax 96 MG/ML Oral SolutionSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130602772004097GTIN-13: 0602772004097
EAN-13: 0602772004097
GTIN-12: 602772004097
UPC-A: 602772004097
GTIN storage (14 digits): 00602772004097
AmproMax_500mL.jpg, AmproMax_3785mL-1-gal.jpg
QR code linkQR Codevetr.com/AmproMax_500mL.jpg, AmproMax_3785mL-1-gal.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86213-772-01Ampromax500 mL in 1 BOTTLE, PLASTICSOLUTION5002
86213-772-02Ampromax3785.4 mL in 1 BOTTLE, PLASTICSOLUTION3785.42

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86213-77286213-772-01, 86213-772-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMPROLIUM95CO6N199QACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.