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Niacin

NDC 59651-019 · Aurobindo Pharma Limited

Generic nameNiacin
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)NIACIN
Strength750 mg/1
Pharmacologic classNicotinic Acid [EPC], Nicotinic Acids [CS]
Marketing categoryANDA

Packages

59651-019-05 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-019-05)

59651-019-18 — 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-019-18)

59651-019-90 — 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-019-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-187 — Niacin, 33342-189 — Niacin, 47335-539 — NIACIN, 47335-613 — NIACIN, 47335-614 — NIACIN, 50268-584 — Niacin, 51407-267 — Niacin, 51407-268 — Niacin, 52747-711 — Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid, 59651-018 — Niacin, 59651-020 — Niacin, 62135-497 — Niacin, 62135-498 — Niacin, 62175-320 — Niacin, 62175-322 — Niacin, 65162-321 — Niacin, 65162-322 — Niacin, 65162-323 — Niacin, 68180-222 — NIACIN, 70752-295 — Niacin, +4 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.