Valium - 0140-0005-14 - (diazepam)

Alphabetical Index


Drug Information of Valium

Product NDC: 0140-0005
Proprietary Name: Valium
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 Valium

Product NDC: 0140-0005
Labeler Name: Roche Products Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013263
Marketing Category: NDA
Start Marketing Date: 19631115

Package Information of Valium

Package NDC: 0140-0005-14
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0140-0005-14)

NDC Information of Valium

NDC Code 0140-0005-14
Proprietary Name Valium
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0140-0005-14)
Product NDC 0140-0005
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19631115
Marketing Category Name NDA
Labeler Name Roche Products Inc
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Valium


General Information