Home > National Drug Code (NDC) > Chlordiazepoxide Hydrochloride

Chlordiazepoxide Hydrochloride - 43063-046-19 - (Chlordiazepoxide Hydrochloride)

Alphabetical Index


Drug Information of Chlordiazepoxide Hydrochloride

Product NDC: 43063-046
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: 43063-046
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084769
Marketing Category: ANDA
Start Marketing Date: 20101206

Package Information of Chlordiazepoxide Hydrochloride

Package NDC: 43063-046-19
Package Description: 19 CAPSULE in 1 BOTTLE, PLASTIC (43063-046-19)

NDC Information of Chlordiazepoxide Hydrochloride

NDC Code 43063-046-19
Proprietary Name Chlordiazepoxide Hydrochloride
Package Description 19 CAPSULE in 1 BOTTLE, PLASTIC (43063-046-19)
Product NDC 43063-046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101206
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name CHLORDIAZEPOXIDE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Chlordiazepoxide Hydrochloride


General Information