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Chlordiazepoxide Hydrochloride - 54868-2361-3 - (Chlordiazepoxide Hydrochloride)

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Drug Information of Chlordiazepoxide Hydrochloride

Product NDC: 54868-2361
Proprietary Name: Chlordiazepoxide Hydrochloride
Non Proprietary Name: Chlordiazepoxide Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Chlordiazepoxide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Chlordiazepoxide Hydrochloride

Product NDC: 54868-2361
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084769
Marketing Category: ANDA
Start Marketing Date: 19930324

Package Information of Chlordiazepoxide Hydrochloride

Package NDC: 54868-2361-3
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (54868-2361-3)

NDC Information of Chlordiazepoxide Hydrochloride

NDC Code 54868-2361-3
Proprietary Name Chlordiazepoxide Hydrochloride
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (54868-2361-3)
Product NDC 54868-2361
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19930324
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CHLORDIAZEPOXIDE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Chlordiazepoxide Hydrochloride


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