Alprazolam - 47335-605-83 - (Alprazolam)

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Drug Information of Alprazolam

Product NDC: 47335-605
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): 1    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 47335-605
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090082
Marketing Category: ANDA
Start Marketing Date: 20100618

Package Information of Alprazolam

Package NDC: 47335-605-83
Package Description: 30 TABLET in 1 BOTTLE (47335-605-83)

NDC Information of Alprazolam

NDC Code 47335-605-83
Proprietary Name Alprazolam
Package Description 30 TABLET in 1 BOTTLE (47335-605-83)
Product NDC 47335-605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100618
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information