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Pyrazinamide - 67253-660-50 - (Pyrazinamide)

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Drug Information of Pyrazinamide

Product NDC: 67253-660
Proprietary Name: Pyrazinamide
Non Proprietary Name: Pyrazinamide
Active Ingredient(s): 500    mg/1 & nbsp;   Pyrazinamide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pyrazinamide

Product NDC: 67253-660
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080157
Marketing Category: ANDA
Start Marketing Date: 19710603

Package Information of Pyrazinamide

Package NDC: 67253-660-50
Package Description: 500 TABLET in 1 BOTTLE (67253-660-50)

NDC Information of Pyrazinamide

NDC Code 67253-660-50
Proprietary Name Pyrazinamide
Package Description 500 TABLET in 1 BOTTLE (67253-660-50)
Product NDC 67253-660
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pyrazinamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19710603
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, Inc.
Substance Name PYRAZINAMIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Pyrazinamide


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