Alprazolam - 49349-206-02 - (Alprazolam)

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Drug Information of Alprazolam

Product NDC: 49349-206
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: 49349-206
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074174
Marketing Category: ANDA
Start Marketing Date: 20110421

Package Information of Alprazolam

Package NDC: 49349-206-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-206-02)

NDC Information of Alprazolam

NDC Code 49349-206-02
Proprietary Name Alprazolam
Package Description 30 TABLET in 1 BLISTER PACK (49349-206-02)
Product NDC 49349-206
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110421
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ALPRAZOLAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information