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Chlordiazepoxide Hydrochloride - 51079-375-20 - (Chlordiazepoxide Hydrochloride)

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Drug Information of Chlordiazepoxide Hydrochloride

Product NDC: 51079-375
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: 51079-375
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083116
Marketing Category: ANDA
Start Marketing Date: 20120810

Package Information of Chlordiazepoxide Hydrochloride

Package NDC: 51079-375-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-375-20) > 1 CAPSULE in 1 BLISTER PACK (51079-375-01)

NDC Information of Chlordiazepoxide Hydrochloride

NDC Code 51079-375-20
Proprietary Name Chlordiazepoxide Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-375-20) > 1 CAPSULE in 1 BLISTER PACK (51079-375-01)
Product NDC 51079-375
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120810
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
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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