Alprazolam - 68788-9727-6 - (Alprazolam)

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Drug Information of Alprazolam

Product NDC: 68788-9727
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): 1    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 68788-9727
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078387
Marketing Category: ANDA
Start Marketing Date: 20121115

Package Information of Alprazolam

Package NDC: 68788-9727-6
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9727-6)

NDC Information of Alprazolam

NDC Code 68788-9727-6
Proprietary Name Alprazolam
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9727-6)
Product NDC 68788-9727
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20121115
Marketing Category Name ANDA
Labeler Name Preferred 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