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Loperamide Hydrochloride - 54868-2118-0 - (loperamide hydrochloride)

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Drug Information of Loperamide Hydrochloride

Product NDC: 54868-2118
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Loperamide Hydrochloride

Product NDC: 54868-2118
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072741
Marketing Category: ANDA
Start Marketing Date: 19960620

Package Information of Loperamide Hydrochloride

Package NDC: 54868-2118-0
Package Description: 10 CAPSULE in 1 BOTTLE (54868-2118-0)

NDC Information of Loperamide Hydrochloride

NDC Code 54868-2118-0
Proprietary Name Loperamide Hydrochloride
Package Description 10 CAPSULE in 1 BOTTLE (54868-2118-0)
Product NDC 54868-2118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loperamide hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19960620
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Loperamide Hydrochloride


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