Diazepam - 54868-2126-5 - (Diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 54868-2126
Proprietary Name: Diazepam
Non Proprietary Name: Diazepam
Active Ingredient(s): 2    mg/1 & nbsp;   Diazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diazepam

Product NDC: 54868-2126
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071307
Marketing Category: ANDA
Start Marketing Date: 20080723

Package Information of Diazepam

Package NDC: 54868-2126-5
Package Description: 10 TABLET in 1 BOTTLE (54868-2126-5)

NDC Information of Diazepam

NDC Code 54868-2126-5
Proprietary Name Diazepam
Package Description 10 TABLET in 1 BOTTLE (54868-2126-5)
Product NDC 54868-2126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080723
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DIAZEPAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information