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
- 43598-010_dc9f1708-68a6-cb89-36c5-4e5fdb30100e
- Product NDC
- 43598-010
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Omeprazole and Sodium Bicarbonate
- Labeler
- Dr. Reddy's Laboratories Inc.,
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240715
- Source listing expiry
- 20261231
Source-listed ingredients
- OMEPRAZOLE — 20 mg/1
- SODIUM BICARBONATE — 1680 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 PACKET in 1 CARTON (43598-010-01) / 1 POWDER, FOR SUSPENSION in 1 PACKET · 43598-010-01
- 14 PACKET in 1 CARTON (43598-010-14) / 1 POWDER, FOR SUSPENSION in 1 PACKET · 43598-010-14
- 28 PACKET in 1 CARTON (43598-010-28) / 1 POWDER, FOR SUSPENSION in 1 PACKET · 43598-010-28
- 42 PACKET in 1 CARTON (43598-010-42) / 1 POWDER, FOR SUSPENSION in 1 PACKET · 43598-010-42
Source and coverage
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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.
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