Isoniazid - 0185-4351-10 - (Isoniazid)

Alphabetical Index


Drug Information of Isoniazid

Product NDC: 0185-4351
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: 0185-4351
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008678
Marketing Category: NDA
Start Marketing Date: 19781211

Package Information of Isoniazid

Package NDC: 0185-4351-10
Package Description: 1000 TABLET in 1 BOTTLE (0185-4351-10)

NDC Information of Isoniazid

NDC Code 0185-4351-10
Proprietary Name Isoniazid
Package Description 1000 TABLET in 1 BOTTLE (0185-4351-10)
Product NDC 0185-4351
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isoniazid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19781211
Marketing Category Name NDA
Labeler Name Eon Labs, Inc.
Substance Name ISONIAZID
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Isoniazid


General Information