Isoniazid - 49349-786-02 - (Isoniazid)

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Drug Information of Isoniazid

Product NDC: 49349-786
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: 49349-786
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080937
Marketing Category: ANDA
Start Marketing Date: 20110928

Package Information of Isoniazid

Package NDC: 49349-786-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-786-02)

NDC Information of Isoniazid

NDC Code 49349-786-02
Proprietary Name Isoniazid
Package Description 30 TABLET in 1 BLISTER PACK (49349-786-02)
Product NDC 49349-786
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isoniazid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110928
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ISONIAZID
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Isoniazid


General Information