Esomeprazole Magnesium
NDC 57483-225, Esomeprazole Magnesium, capsule, delayed release, from INNOVUS PHARMACEUTICALS, INC..
- Product NDC
- 57483-225
- Status
- Listed
- Labeler
- INNOVUS PHARMACEUTICALS, INC.
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA209339
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/57483-225 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ESOMEPRAZOLE MAGNESIUM DIHYDRATE20 mg/1
Pharmacologic classes
Cytochrome P450 2C19 Inhibitors [MoA]; Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 57483-225-42 | 57483022542 | 3 BOTTLE in 1 CARTON (57483-225-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 57483-225 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/57483-225 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 57483-225. 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.