AMPROL- amprolium solution 
Huvepharma, Inc

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Amprol®
(amprolium)

FRONT PANEL

AMPROL®

(amprolium)

9.6% Oral Solution

Coccidiostat

Water-soluble treatment for coccidiosis

Treats 800 Gallons at 0.012% level

Product # 09568A

Net Contents: 128 fl.oz (1 gal.) (3.785 L)

Active Ingredient: amprolium............9.6%

1022-1814-03 Rev. 09-2022

INDICATIONS FOR USE: AMPROL® (amprolium) 9.6% Oral Solution is intended for the treatment of
coccidiosis in growing chickens, turkeys, and laying hens. If no improvement is noted within 3 days,
have the diagnosis confirmed and follow the instructions of your veterinarian or poultry pathologist.
Losses may result from intercurrent disease or other conditions affecting drug intake which can
contribute to the virulence of coccidiosis under field conditions.

USE DIRECTIONS: Give amprolium at the 0.012% level (8 fl oz per 50 gallons) as soon as coccidiosis is
diagnosed and continue for 3 to 5 days. (In severe outbreaks, give amprolium at the 0.024% level.)
Continue with 0.006% amprolium medicated water for an additional 1 to 2 weeks. No other source of
drinking water should be available to the birds during this time. Use as the sole source of amprolium.

WITHDRAWAL PERIODS: No withdrawal period is required when used according to labeling.

USER SAFETY WARNING: Keep this and all drugs out of the reach of children. NOT FOR HUMAN USE.

PRECAUTIONS: FOR ORAL USE IN ANIMALS ONLY.
MAY CAUSE EYE IRRITATION. For irritation, flush with plenty of water; get medical attention.
Restricted Drug (California) - Use Only as Directed.

STORAGE: Store between 5º - 25ºC (41º - 77ºF) with brief excursions to 40ºC.
Benzoic acid 0.1% added as preservative.

Contact Huvepharma Inc. at 1-877-994-4883 or http://www.huvepharma.us. For additional
information about reporting side effects for animal drugs, contact FDA at 1-888-FDA-VETS or
http://www.fda.gov/reportanimalae.

Distributed by:
Huvepharma, Inc.
525 Westpark Drive, Suite 230
Peachtree City, GA 30269
                                                                        ®AMPROL is a registered
Approved by FDA under NADA # 013-149    trademark of Huvepharma, Inc

               FOR ANIMAL USE ONLY

            To prepare 50 Gallons of Medicated Water

DOSAGE LEVELMIXING DIRECTIONS
0.024%Add 1 pint (16 fluid ounces) of AMPROL (amprolium) 9.6% Oral Solution to about 5 gallons of water in a 50-gallon medication barrel.  Stir, then add water to the 50-gallon mark. Stir thoroughly.
0.012%Follow same directions as above but use 1/2 pint (8 fluid ounces) of AMPROL 9.6% Oral Solution
0.006%Follow same directions as above but use 4 fluid ounces of AMPROL 9.6% Oral Solution

            For Automatic Water Proportioners
For automatic water proportioners that meter 1 fluid ounce
of stock solution per gallon of drinking water.

DOSAGE LEVELAMPROL 9.6% ORAL SOLUTION PER
GALLON OF STOCK SOLUTION
0.024%
0.012%
0.006%
41 fl oz
20.5 fl oz
10.25 fl oz

Note: Make drinking water fresh daily. Stock solutions for proportioners may be stored
in a clean, closed labeled container for up to 3 days.

See bottle for Lot No.
and Exp. Date

Take Time Image

Amprol 1 gallon bottle

AMPROL 
amprolium solution
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:23243-6681
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMPROLIUM (UNII: 95CO6N199Q) (AMPROLIUM ION - UNII:H2T307KMZR) AMPROLIUM96 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:23243-6681-24 in 1 BOX
13785 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA01314906/29/2009
Labeler - Huvepharma, Inc (619153559)
Registrant - Huvepharma EOOD (552691651)
Establishment
NameAddressID/FEIBusiness Operations
Huvepharma, Inc - St. Louis883128204analysis, label, manufacture, medicated animal feed manufacture, pack

Revised: 2/2023
Document Id: 75484333-d964-4040-b0d3-b7308733696b
Set id: 831141f7-9458-4de5-9ddc-d183e220fbb7
Version: 6
Effective Time: 20230228
 
Huvepharma, Inc