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"50419-751-01" National Drug Code (NDC)

Lampit 1 BOTTLE in 1 CARTON (50419-751-01) / 100 TABLET, FILM COATED in 1 BOTTLE
(Bayer Healthcare Pharmaceuticals INC.)

NDC Code50419-751-01
Package Description1 BOTTLE in 1 CARTON (50419-751-01) / 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC50419-751
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLampit
Non-Proprietary NameNifurtimox
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20201001
Marketing Category NameNDA
Application NumberNDA213464
ManufacturerBayer Healthcare Pharmaceuticals INC.
Substance NameNIFURTIMOX
Strength120
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50419-751-01





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