NDC 71288-037 – Xenleta

Lefamulin Acetate 600 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71288-037

Product details

Brand name
Xenleta
Generic name
Lefamulin acetate
Labeler
Meitheal Pharmaceuticals Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
NDA · NDA211672
Marketed since
September 9, 2019
Listing expires
December 31, 2027
Pharmacologic class
Pleuromutilin Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Xenleta →

Package NDC codes (1)

Package NDCDescriptionSince
71288-037-1010 TABLET, COATED in 1 BLISTER PACK (71288-037-10)Sep 9, 2019

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