Isoniazid - 49349-318-02 - (Isoniazid)

Alphabetical Index


Drug Information of Isoniazid

Product NDC: 49349-318
Proprietary Name: Isoniazid
Non Proprietary Name: Isoniazid
Active Ingredient(s): 100    mg/1 & nbsp;   Isoniazid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Isoniazid

Product NDC: 49349-318
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008678
Marketing Category: NDA
Start Marketing Date: 20110621

Package Information of Isoniazid

Package NDC: 49349-318-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-318-02)

NDC Information of Isoniazid

NDC Code 49349-318-02
Proprietary Name Isoniazid
Package Description 30 TABLET in 1 BLISTER PACK (49349-318-02)
Product NDC 49349-318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isoniazid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110621
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name ISONIAZID
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Isoniazid


General Information