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Methylprednisolone sodium succinate

NDC 70518-3684, Methylprednisolone sodium succinate, injection, from REMEDYREPACK INC..

Product NDC
70518-3684
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212396
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3684 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE SODIUM SUCCINATE125 mg/2mL

Pharmacologic classes

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

Package NDCNDC-11Package
70518-3684-07051836840025 VIAL, SINGLE-DOSE in 1 CARTON (70518-3684-0) / 2 mL in 1 VIAL, SINGLE-DOSE (70518-3684-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f339882f-c380-4022-bdcd-94556a7926aa

Use it

Look up 70518-3684 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3684 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3684. 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.