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Loperamide Hydrochloride - 53329-664-57 - (Loperamide Hydrochloride)

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Drug Information of Loperamide Hydrochloride

Product NDC: 53329-664
Proprietary Name: Loperamide Hydrochloride
Non Proprietary Name: Loperamide Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Loperamide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Loperamide Hydrochloride

Product NDC: 53329-664
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074091
Marketing Category: ANDA
Start Marketing Date: 19930201

Package Information of Loperamide Hydrochloride

Package NDC: 53329-664-57
Package Description: 12 TABLET in 1 BLISTER PACK (53329-664-57)

NDC Information of Loperamide Hydrochloride

NDC Code 53329-664-57
Proprietary Name Loperamide Hydrochloride
Package Description 12 TABLET in 1 BLISTER PACK (53329-664-57)
Product NDC 53329-664
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930201
Marketing Category Name ANDA
Labeler Name Medline Industries, Inc.
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loperamide Hydrochloride


General Information