Diazepam - 51079-285-20 - (diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 51079-285
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: 51079-285
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070325
Marketing Category: ANDA
Start Marketing Date: 20091120

Package Information of Diazepam

Package NDC: 51079-285-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-285-20) > 1 TABLET in 1 BLISTER PACK (51079-285-01)

NDC Information of Diazepam

NDC Code 51079-285-20
Proprietary Name Diazepam
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-285-20) > 1 TABLET in 1 BLISTER PACK (51079-285-01)
Product NDC 51079-285
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 UDL Laboratories, Inc.
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information