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Esomeprazole Magnesium

NDC 72789-352 · PD-Rx Pharmaceuticals, Inc.

Generic nameEsomeprazole Magnesium
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)ESOMEPRAZOLE MAGNESIUM DIHYDRATE
Strength20 mg/1
Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

72789-352-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-352-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68382-848 — Esomeprazole Magnesium, 68382-849 — Esomeprazole Magnesium, 69097-507 — Esomeprazole magnesium, 69097-508 — Esomeprazole magnesium, 69097-528 — Esomeprazole magnesium, 69097-529 — Esomeprazole magnesium, 69842-248 — Esomeprazole Magnesium, 69842-703 — esomeprazole magnesium, 70000-0695 — Esomeprazole Magnesium, 70000-0731 — ESOMEPRAZOLE MAGNESIUM, 70771-1391 — Esomeprazole Magnesium, 70771-1392 — Esomeprazole Magnesium, 70771-1493 — esomeprazole magnesium, 70771-1494 — esomeprazole magnesium, 71335-0807 — Esomeprazole Magnesium, 71335-1335 — esomeprazole magnesium, 71335-1368 — esomeprazole magnesium, 72476-500 — Esomeprazole Magnesium, 79903-293 — esomeprazole magnesium dihydrate, 80425-0111 — Esomeprazole Magnesium, +24 more

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