Omeprazole

NDC 43598-286 · Dr. Reddys Laboratories Inc

Generic nameOmeprazole

Dosage formTABLET, DELAYED RELEASE

RouteORAL

Active ingredient(s)OMEPRAZOLE

Strength20 mg/1

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

Marketing categoryANDA

Packages

43598-286-25 2 BLISTER PACK in 1 CARTON (43598-286-25) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

43598-286-27 2 BOTTLE in 1 CARTON (43598-286-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)

43598-286-32 2 BLISTER PACK in 1 CARTON (43598-286-32) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (43598-286-70)

43598-286-33 3 BOTTLE in 1 CARTON (43598-286-33) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)

43598-286-37 3 BLISTER PACK in 1 CARTON (43598-286-37) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

43598-286-52 14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)

43598-286-74 1 BLISTER PACK in 1 CARTON (43598-286-74) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

42507-164 — omeprazole, 42507-414 — Omeprazole, 42507-915 — Omeprazole, 42708-158 — Omeprazole, 42708-159 — Omeprazole, 42708-170 — Omeprazole, 42708-199 — Omeprazole, 43063-743 — Omeprazole, 43353-829 — omeprazole, 43598-010 — Omeprazole and Sodium Bicarbonate, 43598-307 — Omeprazole and Sodium Bicarbonate, 43598-841 — Omeprazole, 45802-888 — Omeprazole, 46122-029 — Omeprazole, 46122-281 — Omeprazole, 46122-616 — omeprazole, 46122-739 — Omeprazole, 49035-119 — Omeprazole, 49035-915 — Omeprazole, 49999-265 — Omeprazole, +295 more

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