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Methylprednisolone Sodium Succinate

NDC 70121-1000, Methylprednisolone, injection, powder, lyophilized, for solution, from Amneal Pharmaceuticals LLC.

Product NDC
70121-1000
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207549
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1000 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE SODIUM SUCCINATE40 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
70121-1000-57012110000525 VIAL in 1 CARTON (70121-1000-5) / 1 mL in 1 VIAL (70121-1000-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e86fbda8-00e4-4d54-841a-59dea6c15e70

Use it

Look up 70121-1000 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1000 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70121-1000. 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.