Methylprednisolone
NDC 76420-041, Methylprednisolone, tablet, from Asclemed USA, Inc..
- Product NDC
- 76420-041
- Status
- Listed
- Labeler
- Asclemed USA, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA040189
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76420-041 \ -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 |
|---|---|---|
| 76420-041-21 | 76420004121 | 21 TABLET in 1 BLISTER PACK (76420-041-21) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/8bfdc471-54f7-4298-ba2f-e5c1f6c48456
Use it
Look up 76420-041 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76420-041 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76420-041. 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.