NDC 65162-323 – Niacin

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

Human Prescription Drug

Product NDC65162-323

Product details

Brand name
Niacin
Generic name
Niacin
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203578
Marketed since
July 27, 2015
Listing expires
December 31, 2027
Pharmacologic class
Nicotinic Acid

Active ingredients

Uses, dosage, side effects and warnings for Niacin →

Package NDC codes (3)

Package NDCDescriptionSince
65162-323-0330 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-323-03)Jul 27, 2015
65162-323-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-323-09)Jul 27, 2015
65162-323-50500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-323-50)Jul 27, 2015

Other Niacin products