Diazepam - 68084-359-01 - (Diazepam)

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Drug Information of Diazepam

Product NDC: 68084-359
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: 68084-359
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071135
Marketing Category: ANDA
Start Marketing Date: 20091013

Package Information of Diazepam

Package NDC: 68084-359-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-359-01) > 10 TABLET in 1 BLISTER PACK (68084-359-11)

NDC Information of Diazepam

NDC Code 68084-359-01
Proprietary Name Diazepam
Package Description 10 BLISTER PACK in 1 CARTON (68084-359-01) > 10 TABLET in 1 BLISTER PACK (68084-359-11)
Product NDC 68084-359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091013
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information