Package 50419-751-01

Brand: lampit

Generic: nifurtimox
NDC Package

Package Facts

Identity

Package NDC 50419-751-01
Digits Only 5041975101
Product NDC 50419-751
Product ID 50419-751_9b14492a-5ae2-4d0a-85c0-212636daf8cd
Description

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

Marketing

Marketing Status
Marketed Since 2020-10-01
Brand lampit
Generic nifurtimox
Sample Package No

Linked Drug Pages (1)

LAMPIT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9b14492a-5ae2-4d0a-85c0-212636daf8cd", "openfda": {"unii": ["M84I3K7C2O"], "rxcui": ["430512", "2395842", "2397991", "2397994"], "spl_set_id": ["90d09714-a8b1-4696-8ada-f99dc54d0721"], "manufacturer_name": ["Bayer HealthCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50419-751-01)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50419-751-01", "marketing_start_date": "20201001"}], "brand_name": "LAMPIT", "product_id": "50419-751_9b14492a-5ae2-4d0a-85c0-212636daf8cd", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50419-751", "generic_name": "nifurtimox", "labeler_name": "Bayer HealthCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LAMPIT", "active_ingredients": [{"name": "NIFURTIMOX", "strength": "120 mg/1"}], "application_number": "NDA213464", "marketing_category": "NDA", "marketing_start_date": "20201001", "listing_expiration_date": "20271231"}