DIAZEPAM - 16590-070-90 - (DIAZEPAM)

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Drug Information of DIAZEPAM

Product NDC: 16590-070
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: 16590-070
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077749
Marketing Category: ANDA
Start Marketing Date: 20060331

Package Information of DIAZEPAM

Package NDC: 16590-070-90
Package Description: 90 TABLET in 1 BOTTLE (16590-070-90)

NDC Information of DIAZEPAM

NDC Code 16590-070-90
Proprietary Name DIAZEPAM
Package Description 90 TABLET in 1 BOTTLE (16590-070-90)
Product NDC 16590-070
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIAZEPAM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060331
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of DIAZEPAM


General Information