Diazepam - 54569-0949-1 - (diazepam)

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Drug Information of Diazepam

Product NDC: 54569-0949
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: 54569-0949
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077749
Marketing Category: ANDA
Start Marketing Date: 20060331

Package Information of Diazepam

Package NDC: 54569-0949-1
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (54569-0949-1)

NDC Information of Diazepam

NDC Code 54569-0949-1
Proprietary Name Diazepam
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (54569-0949-1)
Product NDC 54569-0949
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 A-S Medication Solutions LLC
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information