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RABEPRAZOLE SODIUM

NDC 72189-169 · DIRECT RX

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

72189-169-30 — 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-30)

72189-169-60 — 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-60)

72189-169-90 — 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 72888-059 — rabeprazole sodium, 76420-107 — Rabeprazole Sodium, 76420-223 — rabeprazole sodium, 76420-818 — Rabeprazole Sodium, 80425-0094 — Rabeprazole Sodium, 80425-0134 — Rabeprazole Sodium, 80425-0363 — rabeprazole sodium, 80425-0449 — rabeprazole sodium, 80725-243 — rabeprazole sodium, 85509-1443 — 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.