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Chlordiazepoxide Hydrochloride - 49349-915-02 - (Chlordiazepoxide Hydrochloride)

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Drug Information of Chlordiazepoxide Hydrochloride

Product NDC: 49349-915
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: 49349-915
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084769
Marketing Category: ANDA
Start Marketing Date: 20120314

Package Information of Chlordiazepoxide Hydrochloride

Package NDC: 49349-915-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-915-02)

NDC Information of Chlordiazepoxide Hydrochloride

NDC Code 49349-915-02
Proprietary Name Chlordiazepoxide Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-915-02)
Product NDC 49349-915
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120314
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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