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NIACIN

NDC 47335-613 · Sun Pharmaceutical Industries, Inc.

Generic nameNIACIN
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)NIACIN
Strength1000 mg/1
Pharmacologic classNicotinic Acid [EPC], Nicotinic Acids [CS]
Marketing categoryANDA

Packages

47335-613-08 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-08)

47335-613-18 — 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-18)

47335-613-81 — 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-81)

47335-613-83 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-83)

47335-613-88 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-187 — Niacin, 33342-189 — Niacin, 47335-539 — 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, 59651-019 — 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.