Amprol description, usages, side effects, indications, overdosage, supplying and lots more!

Amprol

Huvepharma, Inc.
Huvepharma AD

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
AMPROL SOLUBLE POWDER

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

INDICATIONS

AMPROL 128 (amprolium) 20% Soluble Powder is intended for the treatment of
coccidiosis in growing chickens, turkeys and laying hens.

USE DIRECTIONS

USE DIRECTIONS: Give amprolium at the 0.012% level (10 oz AMPROL 128 20%
Soluble Powder per 128 Gallons) as soon as coccidiosis is diagnosed and continue for
three to five 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.

CAUTION

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 cocidiosis under field conditions.


NOT FOR HUMAN USE.
Restricted Drug - Use Only as Directed (California)
Keep this and all drugs out of the reach of children.




MIXING AND DOSAGE ADMINISTRATION



PREMEASURED FOR AUTOMATIC
WATER PROPORTIONERS

For Automatic Water Proportioners





         Dissolve AMPROL 128
                                   (amprolium) 20% Soluble Powder
To prepare                           In one gallon of water
dosage levels of:               (Makes 1 gallon of stock solution)







DOSAGE LEVEL MIXING DIRECTIONS





Stir thoroughly.















STORAGE

STORAGE: Store between 5o - 25oC (41o - 77oF) with brief excursions to 40oC (104oF)

Amprol 128 Label Image

Amprol 128 Label Image


Amprol 128 Label Image

Amprol

Amprolium POWDER

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:23243-9709
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AMPROLIUM AMPROLIUM 0.2 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 283.5 in 1 POUCH
2 NDC:23243-9709-3 24 in 1 PAIL

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NADA NADA033165 2009-06-29


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Be sure to consult your doctor before taking any medication!
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