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methylprednisolone

NDC 70771-1348, methylprednisolone, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1348
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206751
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1348 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPREDNISOLONE4 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70771-1348-170771134801100 TABLET in 1 BOTTLE (70771-1348-1)
70771-1348-3707711348031 BLISTER PACK in 1 CARTON (70771-1348-3) / 21 TABLET in 1 BLISTER PACK
70771-1348-570771134805500 TABLET in 1 BOTTLE (70771-1348-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fe9c15b5-4264-45f1-87b5-f7e1d6e6ddee

Use it

Look up 70771-1348 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1348 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1348. 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.