Isoniazid - 63629-1422-4 - (Isoniazid)

Alphabetical Index


Drug Information of Isoniazid

Product NDC: 63629-1422
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: 63629-1422
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087425
Marketing Category: ANDA
Start Marketing Date: 19810714

Package Information of Isoniazid

Package NDC: 63629-1422-4
Package Description: 35 TABLET in 1 BOTTLE (63629-1422-4)

NDC Information of Isoniazid

NDC Code 63629-1422-4
Proprietary Name Isoniazid
Package Description 35 TABLET in 1 BOTTLE (63629-1422-4)
Product NDC 63629-1422
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isoniazid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19810714
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ISONIAZID
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Isoniazid


General Information