Skip to main content

Ranolazine

NDC 70625-206 · SunGen Pharma LLC

Generic nameRANOLAZINE
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)RANOLAZINE
Strength500 mg/1
Pharmacologic classAnti-anginal [EPC], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
Marketing categoryANDA

Packages

70625-206-00 — 29125 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOX (70625-206-00)

70625-206-01 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-206-01)

70625-206-02 — 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-206-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63304-018 — Ranolazine, 63629-4874 — Ranolazine, 67877-525 — Ranolazine, 67877-526 — Ranolazine, 68180-354 — RANOLAZINE, 68180-355 — RANOLAZINE, 68462-319 — RANOLAZINE, 68462-320 — RANOLAZINE, 69367-293 — Ranolazine, 69367-294 — Ranolazine, 70625-207 — RANOLAZINE, 70756-703 — Ranolazine, 70756-704 — Ranolazine, 70771-1499 — Ranolazine, 70771-1500 — Ranolazine, 71205-867 — Ranolazine, 71205-868 — Ranolazine, 71335-2556 — RANOLAZINE, 71610-518 — RANOLAZINE, 71610-971 — RANOLAZINE, +34 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.