Omeprazole and sodium bicarbonate
NDC 37808-732, Omeprazole, sodium bicarbonate, capsule, gelatin coated, from H E B.
- Product NDC
- 37808-732
- Status
- Listed
- Labeler
- H E B
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA201361
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/37808-732 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OMEPRAZOLE20 mg/1
- SODIUM BICARBONATE1100 mg/1
Pharmacologic classes
Cytochrome 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]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 37808-732-01 | 37808073201 | 1 BOTTLE in 1 CARTON (37808-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE |
| 37808-732-03 | 37808073203 | 3 BOTTLE in 1 CARTON (37808-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 37808-732 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/37808-732 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 37808-732. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.