up and up esomeprazole magnesium

NDC 11673-898 · Target Corporation

Generic nameEsomeprazole

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)ESOMEPRAZOLE

Strength20 mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Marketing categoryANDA

Packages

11673-898-01 — 1 BOTTLE in 1 CARTON (11673-898-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

11673-898-03 — 3 BOTTLE in 1 CARTON (11673-898-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

FDA lists these products with the same active ingredient.

0113-0651 — esomeprazole, 0113-0898 — Esomeprazole, 0113-2022 — esomeprazole, 0363-1699 — esomeprazole magnesium dihydrate, 0363-7223 — esomeprazole, 11822-0024 — esomeprazole, 11822-0898 — Esomeprazole, 21130-088 — Esomeprazole, 21130-714 — esomeprazole, 30142-273 — esomeprazole, 33342-306 — esomeprazole, 33342-307 — esomeprazole, 37808-719 — esomeprazole, 41250-900 — Esomeprazole, 41520-727 — Esomeprazole, 42507-898 — Esomeprazole, 46122-641 — esomeprazole, 49035-921 — Esomeprazole, 51316-220 — esomeprazole, 55301-898 — Esomeprazole, +15 more

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