Alprazolam - 0603-2127-02 - (alprazolam)

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Drug Information of Alprazolam

Product NDC: 0603-2127
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: 0603-2127
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078491
Marketing Category: ANDA
Start Marketing Date: 20080925

Package Information of Alprazolam

Package NDC: 0603-2127-02
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (0603-2127-02)

NDC Information of Alprazolam

NDC Code 0603-2127-02
Proprietary Name Alprazolam
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (0603-2127-02)
Product NDC 0603-2127
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 Qualitest Pharmaceuticals
Substance Name ALPRAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information