Flurazepam - 68788-0408-9 - (Flurazepam Hydrochloride)

Alphabetical Index


Drug Information of Flurazepam

Product NDC: 68788-0408
Proprietary Name: Flurazepam
Non Proprietary Name: Flurazepam Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Flurazepam Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Flurazepam

Product NDC: 68788-0408
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071108
Marketing Category: ANDA
Start Marketing Date: 20120127

Package Information of Flurazepam

Package NDC: 68788-0408-9
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC (68788-0408-9)

NDC Information of Flurazepam

NDC Code 68788-0408-9
Proprietary Name Flurazepam
Package Description 90 CAPSULE in 1 BOTTLE, PLASTIC (68788-0408-9)
Product NDC 68788-0408
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flurazepam Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120127
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name FLURAZEPAM HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Flurazepam


General Information