Diazepam - 55289-091-12 - (Diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 55289-091
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: 55289-091
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071135
Marketing Category: ANDA
Start Marketing Date: 19870203

Package Information of Diazepam

Package NDC: 55289-091-12
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (55289-091-12)

NDC Information of Diazepam

NDC Code 55289-091-12
Proprietary Name Diazepam
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (55289-091-12)
Product NDC 55289-091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19870203
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information