Diazepam - 21695-265-15 - (Diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 21695-265
Proprietary Name: Diazepam
Non Proprietary Name: Diazepam
Active Ingredient(s): 10    mg/1 & nbsp;   Diazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diazepam

Product NDC: 21695-265
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071322
Marketing Category: ANDA
Start Marketing Date: 20091109

Package Information of Diazepam

Package NDC: 21695-265-15
Package Description: 15 TABLET in 1 BOTTLE (21695-265-15)

NDC Information of Diazepam

NDC Code 21695-265-15
Proprietary Name Diazepam
Package Description 15 TABLET in 1 BOTTLE (21695-265-15)
Product NDC 21695-265
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091109
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name DIAZEPAM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information