Diazepam - 76237-144-39 - (Diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 76237-144
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: 76237-144
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071321
Marketing Category: ANDA
Start Marketing Date: 20111013

Package Information of Diazepam

Package NDC: 76237-144-39
Package Description: 30 TABLET in 1 BLISTER PACK (76237-144-39)

NDC Information of Diazepam

NDC Code 76237-144-39
Proprietary Name Diazepam
Package Description 30 TABLET in 1 BLISTER PACK (76237-144-39)
Product NDC 76237-144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111013
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information