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ALPRAZOLAM EXTENDED-RELEASE - 64980-141-06 - (ALPRAZOLAM)

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Drug Information of ALPRAZOLAM EXTENDED-RELEASE

Product NDC: 64980-141
Proprietary Name: ALPRAZOLAM EXTENDED-RELEASE
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 EXTENDED-RELEASE

Product NDC: 64980-141
Labeler Name: Rising Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077996
Marketing Category: ANDA
Start Marketing Date: 20070328

Package Information of ALPRAZOLAM EXTENDED-RELEASE

Package NDC: 64980-141-06
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-141-06)

NDC Information of ALPRAZOLAM EXTENDED-RELEASE

NDC Code 64980-141-06
Proprietary Name ALPRAZOLAM EXTENDED-RELEASE
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-141-06)
Product NDC 64980-141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALPRAZOLAM
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070328
Marketing Category Name ANDA
Labeler Name Rising Pharmaceuticals Inc
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of ALPRAZOLAM EXTENDED-RELEASE


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