Alprazolam - 55289-962-98 - (alprazolam)

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Drug Information of Alprazolam

Product NDC: 55289-962
Proprietary Name: Alprazolam
Non Proprietary Name: alprazolam
Active Ingredient(s): .25    mg/1 & nbsp;   alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 55289-962
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078491
Marketing Category: ANDA
Start Marketing Date: 20080925

Package Information of Alprazolam

Package NDC: 55289-962-98
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (55289-962-98)

NDC Information of Alprazolam

NDC Code 55289-962-98
Proprietary Name Alprazolam
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (55289-962-98)
Product NDC 55289-962
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080925
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ALPRAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information