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Chlordiazepoxide Hydrochloride - 43547-251-10 - (Chlordiazepoxide Hydrochloride)

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Drug Information of Chlordiazepoxide Hydrochloride

Product NDC: 43547-251
Proprietary Name: Chlordiazepoxide Hydrochloride
Non Proprietary Name: Chlordiazepoxide Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Chlordiazepoxide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Chlordiazepoxide Hydrochloride

Product NDC: 43547-251
Labeler Name: Solco Healthcare US LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085461
Marketing Category: ANDA
Start Marketing Date: 20100515

Package Information of Chlordiazepoxide Hydrochloride

Package NDC: 43547-251-10
Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (43547-251-10)

NDC Information of Chlordiazepoxide Hydrochloride

NDC Code 43547-251-10
Proprietary Name Chlordiazepoxide Hydrochloride
Package Description 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (43547-251-10)
Product NDC 43547-251
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20100515
Marketing Category Name ANDA
Labeler Name Solco Healthcare US LLC
Substance Name CHLORDIAZEPOXIDE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Chlordiazepoxide Hydrochloride


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