NDC 71741-020 – Niacin

Niacin 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71741-020

Product details

Brand name
Niacin
Generic name
Niacin
Labeler
Redmont Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040378
Marketed since
May 3, 2000
Listing expires
December 31, 2026
Pharmacologic class
Nicotinic Acid

Active ingredients

Uses, dosage, side effects and warnings for Niacin →

Package NDC codes (3)

Package NDCDescriptionSince
71741-020-3030 TABLET in 1 BOTTLE (71741-020-30)Dec 12, 2025
71741-020-6060 TABLET in 1 BOTTLE (71741-020-60)Dec 12, 2025
71741-020-9090 TABLET in 1 BOTTLE (71741-020-90)Dec 16, 2021

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