MedPath

Isoniazid

ISONIAZID TABLETS, USP

Approved
Approval ID

ec0df56a-7746-45f2-88dc-a975cf48abc9

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 2, 2010

Manufacturers
FDA

Contract Pharmacy Services-PA

DUNS: 945429777

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Isoniazid

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code67046-333
Application NumberANDA080937
Product Classification
M
Marketing Category
C73584
G
Generic Name
Isoniazid
Product Specifications
Route of AdministrationORAL
Effective DateOctober 20, 2006
FDA Product Classification

INGREDIENTS (1)

isoniazidActive
Quantity: 300 mg in 1 1
Code: V83O1VOZ8L
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.