Methylprednisolone
NDC 70518-4213, methylprednisolone, tablet, from REMEDYREPACK INC..
- Product NDC
- 70518-4213
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA011153
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4213 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPREDNISOLONE4 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4213-0 | 70518421300 | 1 DOSE PACK in 1 CARTON (70518-4213-0) / 21 TABLET in 1 DOSE PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/d2a0e52c-f724-40e6-9d2a-5f1487c104b6
Use it
Look up 70518-4213 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4213 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4213. 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.