United States · FDA National Drug Code directory
Omeprazole and Sodium Bicarbonate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 59779-732_a6fecbac-6464-4363-98b8-700b37d8647f
- Product NDC
- 59779-732
- Form
- CAPSULE, GELATIN COATED
- Composition / generic term
- Omeprazole, sodium bicarbonate
- Labeler
- CVS Pharmacy
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160715
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
- SODIUM BICARBONATE — 1100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (59779-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE · 59779-732-01
- 3 BOTTLE in 1 CARTON (59779-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE · 59779-732-03
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →