Alprazolam - 64376-631-05 - (Alprazolam)

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Drug Information of Alprazolam

Product NDC: 64376-631
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): .5    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 64376-631
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090248
Marketing Category: ANDA
Start Marketing Date: 20101015

Package Information of Alprazolam

Package NDC: 64376-631-05
Package Description: 500 TABLET in 1 BOTTLE (64376-631-05)

NDC Information of Alprazolam

NDC Code 64376-631-05
Proprietary Name Alprazolam
Package Description 500 TABLET in 1 BOTTLE (64376-631-05)
Product NDC 64376-631
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101015
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, Inc.
Substance Name ALPRAZOLAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information