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Flurazepam Hydrochloride - 54868-0092-1 - (flurazepam hydrochloride)

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Drug Information of Flurazepam Hydrochloride

Product NDC: 54868-0092
Proprietary Name: Flurazepam Hydrochloride
Non Proprietary Name: flurazepam hydrochloride
Active Ingredient(s): 15    mg/1 & nbsp;   flurazepam hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Flurazepam Hydrochloride

Product NDC: 54868-0092
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070345
Marketing Category: ANDA
Start Marketing Date: 19950508

Package Information of Flurazepam Hydrochloride

Package NDC: 54868-0092-1
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-0092-1)

NDC Information of Flurazepam Hydrochloride

NDC Code 54868-0092-1
Proprietary Name Flurazepam Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-0092-1)
Product NDC 54868-0092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name flurazepam hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950508
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name FLURAZEPAM HYDROCHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Flurazepam Hydrochloride


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