Diazepam - 0555-0164-06 - (Diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 0555-0164
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: 0555-0164
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070154
Marketing Category: ANDA
Start Marketing Date: 19900630

Package Information of Diazepam

Package NDC: 0555-0164-06
Package Description: 5000 TABLET in 1 BOTTLE (0555-0164-06)

NDC Information of Diazepam

NDC Code 0555-0164-06
Proprietary Name Diazepam
Package Description 5000 TABLET in 1 BOTTLE (0555-0164-06)
Product NDC 0555-0164
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900630
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name DIAZEPAM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information