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Methylprednisolone Sodium Succinate

NDC 70518-4345, Methylprednisolone Sodium Succinate, injection, powder, for solution, from REMEDYREPACK INC..

Product NDC
70518-4345
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203125
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4345 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE SODIUM SUCCINATE125 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-4345-07051843450025 VIAL, SINGLE-DOSE in 1 CARTON (70518-4345-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (70518-4345-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ae524bdb-9fd0-49f9-802d-465a374c175b

Use it

Look up 70518-4345 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4345 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4345. 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.