NDC 50419-750 – Lampit

Nifurtimox 30 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50419-750

Product details

Brand name
Lampit
Generic name
Nifurtimox
Labeler
Bayer HealthCare Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA213464
Marketed since
October 1, 2020
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lampit →

Package NDC codes (1)

Package NDCDescriptionSince
50419-750-011 BOTTLE in 1 CARTON (50419-750-01) / 100 TABLET, FILM COATED in 1 BOTTLEOct 1, 2020

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