Alprazolam - 49884-110-74 - (alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 49884-110
Proprietary Name: Alprazolam
Non Proprietary Name: alprazolam
Active Ingredient(s): .25    mg/1 & nbsp;   alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 49884-110
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078088
Marketing Category: ANDA
Start Marketing Date: 20090109

Package Information of Alprazolam

Package NDC: 49884-110-74
Package Description: 10 BLISTER PACK in 1 CARTON (49884-110-74) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Alprazolam

NDC Code 49884-110-74
Proprietary Name Alprazolam
Package Description 10 BLISTER PACK in 1 CARTON (49884-110-74) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 49884-110
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20090109
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name ALPRAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information