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Rabeprazole Sodium

NDC 70518-2590 · REMEDYREPACK INC.

Generic nameRabeprazole Sodium
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)RABEPRAZOLE SODIUM
Strength20 mg/1
Pharmacologic classProton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

70518-2590-0 — 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2590-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62135-503 — Rabeprazole Sodium, 62175-302 — Rabeprazole Sodium, 63187-259 — Rabeprazole Sodium, 63187-555 — Rabeprazole sodium, 65162-724 — Rabeprazole, 65862-721 — Rabeprazole Sodium, 67877-443 — Rabeprazole Sodium, 68788-4060 — Rabeprazole sodium, 68788-7459 — Rabeprazole Sodium, 68788-8536 — rabeprazole sodium, 70518-3209 — rabeprazole sodium, 71205-292 — Rabeprazole Sodium, 71205-603 — rabeprazole sodium, 71335-0244 — Rabeprazole Sodium, 71335-1100 — Rabeprazole Sodium, 71335-1558 — Rabeprazole Sodium, 71335-2304 — rabeprazole sodium, 72162-2367 — Rabeprazole Sodium, 72162-2503 — rabeprazole sodium, 72189-142 — RABEPRAZOLE SODIUM, +17 more

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