Diazepam - 35356-812-00 - (Diazepam)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 35356-812
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: 35356-812
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071322
Marketing Category: ANDA
Start Marketing Date: 19861210

Package Information of Diazepam

Package NDC: 35356-812-00
Package Description: 100 TABLET in 1 BOTTLE (35356-812-00)

NDC Information of Diazepam

NDC Code 35356-812-00
Proprietary Name Diazepam
Package Description 100 TABLET in 1 BOTTLE (35356-812-00)
Product NDC 35356-812
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19861210
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name DIAZEPAM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information