equate omeprazole and sodium bicarbonate

NDC 79903-013 · WALMART INC.

Generic nameOmeprazole, sodium bicarbonate

Dosage formCAPSULE, GELATIN COATED

RouteORAL

Active ingredient(s)OMEPRAZOLE, SODIUM BICARBONATE

Strength20; 1100 mg/1; mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Marketing categoryANDA

Packages

79903-013-03 — 3 BOTTLE in 1 CARTON (79903-013-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE (79903-013-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76328-221 — SODIUM BICARBONATE, 76328-223 — SODIUM BICARBONATE, 76329-3352 — Sodium Bicarbonate, 76420-055 — Omeprazole, 76420-878 — Omeprazole, 76420-879 — Omeprazole, 77333-829 — Sodium Bicarbonate, 78271-041 — Sodium Bicarbonate, 79481-0075 — omeprazole, 79481-0502 — SODIUM BICARBONATE, SODIUM CHLORIDE, 79903-113 — omeprazole, 79903-305 — Omeprazole, 80425-0070 — Omeprazole, 80425-0071 — Omeprazole, 80425-0109 — Omeprazole, 80425-0169 — Omeprazole, 80425-0415 — Omeprazole, 80425-0504 — Omeprazole, 80513-611 — Sodium Bicarbonate, 80830-2305 — sodium bicarbonate, +494 more

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