Isoniazid - 0555-0071-02 - (Isoniazid)

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Drug Information of Isoniazid

Product NDC: 0555-0071
Proprietary Name: Isoniazid
Non Proprietary Name: Isoniazid
Active Ingredient(s): 300    mg/1 & nbsp;   Isoniazid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Isoniazid

Product NDC: 0555-0071
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080937
Marketing Category: ANDA
Start Marketing Date: 19720901

Package Information of Isoniazid

Package NDC: 0555-0071-02
Package Description: 100 TABLET in 1 BOTTLE (0555-0071-02)

NDC Information of Isoniazid

NDC Code 0555-0071-02
Proprietary Name Isoniazid
Package Description 100 TABLET in 1 BOTTLE (0555-0071-02)
Product NDC 0555-0071
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isoniazid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19720901
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name ISONIAZID
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Isoniazid


General Information