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Methylprednisolone Sodium Succinate

NDC 0143-9182, Methylprednisolone Sodium Succinate, injection, powder, for solution, from Hikma Pharmaceuticals USA Inc..

Product NDC
0143-9182
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202691
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9182 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE SODIUM SUCCINATE1 g/1

Pharmacologic classes

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

Package NDCNDC-11Package
0143-9182-01001439182011 VIAL, MULTI-DOSE in 1 CARTON (0143-9182-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/060bcf13-ce9e-488c-ad43-9d66abb23b18

Use it

Look up 0143-9182 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9182 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0143-9182. 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.