Skip to main content

Rabeprazole Sodium

NDC 65862-721 · Aurobindo Pharma Limited

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

65862-721-30 — 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-721-30)

65862-721-90 — 90 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-721-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-4751 — Rabeprazole Sodium, 50090-6887 — rabeprazole sodium, 51407-184 — Rabeprazole Sodium, 60760-560 — Rabeprazole Sodium, 60760-972 — rabeprazole sodium, 62135-503 — Rabeprazole Sodium, 62175-302 — Rabeprazole Sodium, 63187-259 — Rabeprazole Sodium, 63187-555 — Rabeprazole sodium, 65162-724 — Rabeprazole, 67877-443 — Rabeprazole Sodium, 68788-4060 — Rabeprazole sodium, 68788-7459 — Rabeprazole Sodium, 68788-8536 — rabeprazole sodium, 70518-2590 — Rabeprazole Sodium, 70518-3209 — rabeprazole sodium, 71205-292 — Rabeprazole Sodium, 71205-603 — rabeprazole sodium, 71335-0244 — Rabeprazole Sodium, 71335-1100 — 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.