a d - 55312-224-67 - (Loperamide Hydrochloride)

Alphabetical Index


Drug Information of a d

Product NDC: 55312-224
Proprietary Name: a d
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 a d

Product NDC: 55312-224
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075232
Marketing Category: ANDA
Start Marketing Date: 20030225

Package Information of a d

Package NDC: 55312-224-67
Package Description: 1 BOTTLE in 1 CARTON (55312-224-67) > 48 TABLET, FILM COATED in 1 BOTTLE

NDC Information of a d

NDC Code 55312-224-67
Proprietary Name a d
Package Description 1 BOTTLE in 1 CARTON (55312-224-67) > 48 TABLET, FILM COATED in 1 BOTTLE
Product NDC 55312-224
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030225
Marketing Category Name ANDA
Labeler Name Western Family Foods Inc
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of a d


General Information