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"50419-750-01" National Drug Code (NDC)
Lampit 1 BOTTLE in 1 CARTON (50419-750-01) / 100 TABLET, FILM COATED in 1 BOTTLE
(Bayer Healthcare Pharmaceuticals INC.)
NDC Code
50419-750-01
Package Description
1 BOTTLE in 1 CARTON (50419-750-01) / 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC
50419-750
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lampit
Non-Proprietary Name
Nifurtimox
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20201001
Marketing Category Name
NDA
Application Number
NDA213464
Manufacturer
Bayer Healthcare Pharmaceuticals INC.
Substance Name
NIFURTIMOX
Strength
30
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50419-750-01