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Chlordiazepoxide Hydrochloride - 54569-2095-6 - (Chlordiazepoxide Hydrochloride)

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Drug Information of Chlordiazepoxide Hydrochloride

Product NDC: 54569-2095
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: 54569-2095
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084769
Marketing Category: ANDA
Start Marketing Date: 19760702

Package Information of Chlordiazepoxide Hydrochloride

Package NDC: 54569-2095-6
Package Description: 19 CAPSULE in 1 BOTTLE (54569-2095-6)

NDC Information of Chlordiazepoxide Hydrochloride

NDC Code 54569-2095-6
Proprietary Name Chlordiazepoxide Hydrochloride
Package Description 19 CAPSULE in 1 BOTTLE (54569-2095-6)
Product NDC 54569-2095
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19760702
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
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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