lampit

Generic: nifurtimox

Labeler: bayer healthcare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lampit
Generic Name nifurtimox
Labeler bayer healthcare pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

nifurtimox 120 mg/1

Manufacturer
Bayer HealthCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 50419-751
Product ID 50419-751_9b14492a-5ae2-4d0a-85c0-212636daf8cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA213464
Listing Expiration 2027-12-31
Marketing Start 2020-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50419751
Hyphenated Format 50419-751

Supplemental Identifiers

RxCUI
430512 2395842 2397991 2397994
UNII
M84I3K7C2O

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lampit (source: ndc)
Generic Name nifurtimox (source: ndc)
Application Number NDA213464 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (50419-751-01) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

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

Ingredients (1)

nifurtimox (120 mg/1)

Linked Drug Pages (1)

LAMPIT ndc-match (0.9)

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"}