NDC 50419-751

LAMPIT

Nifurtimox

LAMPIT is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bayer Healthcare Pharmaceuticals Inc.. The primary component is Nifurtimox.

• Product ID: 50419-751_06512bbe-ca2d-436b-92d0-447aff049c3b
• NDC: 50419-751
• Product Type: Human Prescription Drug
• Proprietary Name: LAMPIT
• Generic Name: Nifurtimox
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2020-10-01
• Marketing Category: NDA / NDA
• Application Number: NDA213464
• Labeler Name: Bayer Healthcare Pharmaceuticals INC.
• Substance Name: NIFURTIMOX
• Active Ingredient Strength: 120 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 50419-751-01

1 BOTTLE in 1 CARTON (50419-751-01) > 100 TABLET, FILM COATED in 1 BOTTLE

• Marketing Start Date: 2020-10-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "LAMPIT" or generic name "Nifurtimox"

NDC	Brand Name	Generic Name
50419-750	LAMPIT	nifurtimox
50419-751	LAMPIT	nifurtimox