Esomeprazole Magnesium
NDC 70771-1392, Esomeprazole Magnesium, granule, delayed release, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1392
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- GRANULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206055
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1392 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ESOMEPRAZOLE MAGNESIUM DIHYDRATE40 mg/1
Pharmacologic classes
Cytochrome P450 2C19 Inhibitors [MoA]; Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1392-3 | 70771139203 | 30 GRANULE, DELAYED RELEASE in 1 CARTON (70771-1392-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4cd9e802-c519-4593-bc38-947ad7f9b567
Use it
Look up 70771-1392 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1392 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1392. 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.