Diazepam - 0904-5880-61 - (Diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 0904-5880
Proprietary Name: Diazepam
Non Proprietary Name: Diazepam
Active Ingredient(s): 5    mg/1 & nbsp;   Diazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diazepam

Product NDC: 0904-5880
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071135
Marketing Category: ANDA
Start Marketing Date: 20080605

Package Information of Diazepam

Package NDC: 0904-5880-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-5880-61)

NDC Information of Diazepam

NDC Code 0904-5880-61
Proprietary Name Diazepam
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-5880-61)
Product NDC 0904-5880
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080605
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information