Alprazolam - 59762-0059-1 - (ALPRAZOLAM)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 59762-0059
Proprietary Name: Alprazolam
Non Proprietary Name: ALPRAZOLAM
Active Ingredient(s): 1    mg/1 & nbsp;   ALPRAZOLAM
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 59762-0059
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021434
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20030117

Package Information of Alprazolam

Package NDC: 59762-0059-1
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0059-1)

NDC Information of Alprazolam

NDC Code 59762-0059-1
Proprietary Name Alprazolam
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0059-1)
Product NDC 59762-0059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALPRAZOLAM
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030117
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information