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SOLU-MEDROL

NDC 0009-0758, methylprednisolone sodium succinate, injection, powder, for solution, from Pharmacia & Upjohn Company LLC.

Product NDC
0009-0758
Status
Listed
Labeler
Pharmacia & Upjohn Company LLC
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA011856
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0009-0758 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE SODIUM SUCCINATE500 mg/mL

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
0009-0758-01000090758011 VIAL in 1 CARTON (0009-0758-01) / 8 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cd99be87-c8d9-48d6-a8e5-e081052e3f19

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0009-0758

Use it

Look up 0009-0758 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0009-0758 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0009-0758. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.