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Cyproheptadine Hydrochloride - 54868-1332-7 - (Cyproheptadine Hydrochloride)

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Drug Information of Cyproheptadine Hydrochloride

Product NDC: 54868-1332
Proprietary Name: Cyproheptadine Hydrochloride
Non Proprietary Name: Cyproheptadine Hydrochloride
Active Ingredient(s): 4    mg/1 & nbsp;   Cyproheptadine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cyproheptadine Hydrochloride

Product NDC: 54868-1332
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040537
Marketing Category: ANDA
Start Marketing Date: 20030521

Package Information of Cyproheptadine Hydrochloride

Package NDC: 54868-1332-7
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (54868-1332-7)

NDC Information of Cyproheptadine Hydrochloride

NDC Code 54868-1332-7
Proprietary Name Cyproheptadine Hydrochloride
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (54868-1332-7)
Product NDC 54868-1332
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyproheptadine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030521
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CYPROHEPTADINE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cyproheptadine Hydrochloride


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