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anti diarrheal - 56062-224-53 - (Loperamide Hydrochloride)

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Drug Information of anti diarrheal

Product NDC: 56062-224
Proprietary Name: anti diarrheal
Non Proprietary Name: Loperamide Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Loperamide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of anti diarrheal

Product NDC: 56062-224
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075232
Marketing Category: ANDA
Start Marketing Date: 20030319

Package Information of anti diarrheal

Package NDC: 56062-224-53
Package Description: 2 BLISTER PACK in 1 CARTON (56062-224-53) > 6 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of anti diarrheal

NDC Code 56062-224-53
Proprietary Name anti diarrheal
Package Description 2 BLISTER PACK in 1 CARTON (56062-224-53) > 6 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 56062-224
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030319
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of anti diarrheal


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