United States · FDA National Drug Code directory
Xenleta
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71288-037_b9951406-492b-4420-89cc-24fd655824b3
- Product NDC
- 71288-037
- Form
- TABLET, COATED
- Composition / generic term
- lefamulin acetate
- Labeler
- Meitheal Pharmaceuticals Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20190909
- Source listing expiry
- 20271231
Source-listed ingredients
- LEFAMULIN ACETATE — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, COATED in 1 BLISTER PACK (71288-037-10) · 71288-037-10
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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