NDC 65162-322 – Niacin

Niacin 750 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65162-322

Product details

Brand name
Niacin
Generic name
Niacin
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204178
Marketed since
December 11, 2015
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
65162-322-0330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-322-03)Dec 11, 2015
65162-322-0990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-322-09)Dec 11, 2015
65162-322-50500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-322-50)Dec 11, 2015

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