NDC 47335-613 – Niacin

Niacin 1000 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug 2 recalls

Product NDC47335-613

Product details

Brand name
Niacin
Generic name
Niacin
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA200484
Marketed since
June 27, 2014
Listing expires
December 31, 2026
Pharmacologic class
Nicotinic Acid

Active ingredients

Uses, dosage, side effects and warnings for Niacin →

Package NDC codes (5)

Package NDCDescriptionSince
47335-613-08100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-08)Jun 27, 2014
47335-613-181000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-18)Jun 27, 2014
47335-613-8190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-81)Jun 27, 2014
47335-613-8330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-83)Jun 27, 2014
47335-613-88100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-88)Jun 27, 2014

Recalls mentioning this NDC

Other Niacin products