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Xenleta

NDC 71288-037, lefamulin acetate, tablet, coated, from Meitheal Pharmaceuticals Inc..

Product NDC
71288-037
Status
Listed
Labeler
Meitheal Pharmaceuticals Inc.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA211672
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71288-037 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEFAMULIN ACETATE600 mg/1

Pharmacologic classes

Cytochrome P450 3A Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]; Diterpenes [CS]; Pleuromutilin Antibacterial [EPC]

Package NDCNDC-11Package
71288-037-107128800371010 TABLET, COATED in 1 BLISTER PACK (71288-037-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eb972ea8-7502-422e-84bb-66cb8e93ca06

Use it

Look up 71288-037 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71288-037 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71288-037. 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.