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Methylprednisolone Sodium Succinate

NDC 55150-265, Methylprednisolone Sodium Succinate, injection, powder, lyophilized, for solution, from Eugia US LLC.

Product NDC
55150-265
Status
Listed
Labeler
Eugia US LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207667
DEA schedule
None
Request
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Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE SODIUM SUCCINATE2 g/1

Pharmacologic classes

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

Package NDCNDC-11Package
55150-265-50551500265501 VIAL, SINGLE-DOSE in 1 CARTON (55150-265-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2035f00e-2299-473a-b004-cb93f541cfa9

Use it

Look up 55150-265 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55150-265 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55150-265. 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.