50419-750 : Lampit 30 mg Oral Tablet, Film Coated


NDC50419-750
Labeler: Bayer Healthcare Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Lampit
Dosage Form: Oral Tablet, Film Coated
Application #: NDA213464
Rev. Date: 


NDC Package Codes:

  • 50419-750-01: 1 BOTTLE IN 1 CARTON (50419‑750‑01) > 100 TABLET, FILM COATED IN 1 BOTTLE

Active Ingredients:

  • Nifurtimox

Dosage Strength:

  • 30 mg

Related Products:

Based on records with the same trade name.
  • 50419-751 Lampit 120 mg Oral Tablet, Film Coated by Bayer Healthcare Pharmaceuticals Inc.

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minimizing side affects of Lampit
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