Omeprazole and sodium bicarbonate

NDC 37808-732 · H E B

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

37808-732-01 — 1 BOTTLE in 1 CARTON (37808-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE

37808-732-03 — 3 BOTTLE in 1 CARTON (37808-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-527 — omeprazole, 31722-528 — omeprazole, 36800-121 — Omeprazole, 36800-421 — Aspirin, Citric Acid, Sodium Bicarbonate, 36800-601 — omeprazole, 36800-915 — Omeprazole, 37808-354 — omeprazole, 37808-401 — Omeprazole, 37808-421 — Aspirin, Citric Acid, Sodium Bicarbonate, 37808-540 — Aspirin, Citric Acid, Sodium Bicarbonate, 37808-915 — Omeprazole, 37835-001 — Omeprazole, 40032-090 — POLYETHYLENE GLYCOL-3350 AND ELECTROLYTES, 41163-421 — Aspirin, Citric Acid, Sodium Bicarbonate, 41163-634 — omeprazole, 41163-915 — Omeprazole, 41250-222 — Aspirin, Citric Acid, Sodium Bicarbonate, 41250-349 — omeprazole, 41250-401 — Omeprazole, 41250-915 — Omeprazole, +494 more

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