NDC 71335-2800 – Isoniazid

Isoniazid 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2800

Product details

Brand name
Isoniazid
Generic name
Isoniazid
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA080937
Marketed since
November 1, 2024
Marketing end
February 28, 2028
Pharmacologic class
Antimycobacterial

Active ingredients

Uses, dosage, side effects and warnings for Isoniazid →

Package NDC codes (5)

Package NDCDescriptionSince
71335-2800-1100 TABLET in 1 BOTTLE (71335-2800-1)Oct 13, 2025
71335-2800-230 TABLET in 1 BOTTLE (71335-2800-2)Oct 13, 2025
71335-2800-360 TABLET in 1 BOTTLE (71335-2800-3)Oct 13, 2025
71335-2800-435 TABLET in 1 BOTTLE (71335-2800-4)Oct 13, 2025
71335-2800-590 TABLET in 1 BOTTLE (71335-2800-5)Oct 13, 2025

Other Isoniazid products