Alprazolam - 55289-920-06 - (Alprazolam)

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Drug Information of Alprazolam

Product NDC: 55289-920
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: 55289-920
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074215
Marketing Category: ANDA
Start Marketing Date: 20091231

Package Information of Alprazolam

Package NDC: 55289-920-06
Package Description: 6 TABLET in 1 BOTTLE, PLASTIC (55289-920-06)

NDC Information of Alprazolam

NDC Code 55289-920-06
Proprietary Name Alprazolam
Package Description 6 TABLET in 1 BOTTLE, PLASTIC (55289-920-06)
Product NDC 55289-920
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091231
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information