Diazepam - 55289-092-98 - (diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 55289-092
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: 55289-092
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070325
Marketing Category: ANDA
Start Marketing Date: 20091120

Package Information of Diazepam

Package NDC: 55289-092-98
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (55289-092-98)

NDC Information of Diazepam

NDC Code 55289-092-98
Proprietary Name Diazepam
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (55289-092-98)
Product NDC 55289-092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091120
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name DIAZEPAM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information