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"50419-540-06" National Drug Code (NDC)

Kerendia 10 TABLET, FILM COATED in 1 BLISTER PACK (50419-540-06)
(Bayer HealthCare Pharmaceuticals Inc.)

NDC Code50419-540-06
Package Description10 TABLET, FILM COATED in 1 BLISTER PACK (50419-540-06)
Product NDC50419-540
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameKerendia
Non-Proprietary NameFinerenone
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210709
Marketing Category NameNDA
Application NumberNDA215341
ManufacturerBayer HealthCare Pharmaceuticals Inc.
Substance NameFINERENONE
Strength10
Strength Unitmg/1
Pharmacy ClassesMineralocorticoid Receptor Antagonists [MoA], Nonsteroidal Mineralocorticoid-Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50419-540-06





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