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Chlordiazepoxide Hydrochloride - 55154-5089-0 - (Chlordiazepoxide Hydrochloride)

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Drug Information of Chlordiazepoxide Hydrochloride

Product NDC: 55154-5089
Proprietary Name: Chlordiazepoxide Hydrochloride
Non Proprietary Name: Chlordiazepoxide Hydrochloride
Active Ingredient(s): 10    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: 55154-5089
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083116
Marketing Category: ANDA
Start Marketing Date: 20110401

Package Information of Chlordiazepoxide Hydrochloride

Package NDC: 55154-5089-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5089-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Chlordiazepoxide Hydrochloride

NDC Code 55154-5089-0
Proprietary Name Chlordiazepoxide Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-5089-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-5089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110401
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CHLORDIAZEPOXIDE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Chlordiazepoxide Hydrochloride


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