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methylprednisolone acetate

NDC 25021-821, methylprednisolone acetate, injection, suspension, from Sagent Pharmaceuticals.

Product NDC
25021-821
Status
Listed
Labeler
Sagent Pharmaceuticals
Dosage form
INJECTION, SUSPENSION
Route
INTRA-ARTICULAR, INTRALESIONAL, INTRAMUSCULAR, INTRASYNOVIAL, SOFT TISSUE
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201835
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25021-821 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE ACETATE80 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
25021-821-05250210821051 VIAL in 1 CARTON (25021-821-05) / 5 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f98314ea-a4e4-4f78-987b-3e9b45a08bb4

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=25021-821

Use it

Look up 25021-821 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25021-821 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25021-821. 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.