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"50419-542-02" National Drug Code (NDC)

Kerendia 90 TABLET in 1 BOTTLE, PLASTIC (50419-542-02)
(Bayer HealthCare Pharmaceuticals Inc.)

NDC Code50419-542-02
Package Description90 TABLET in 1 BOTTLE, PLASTIC (50419-542-02)
Product NDC50419-542
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameKerendia
Non-Proprietary NameFinerenone
Dosage FormTABLET
UsageORAL
Start Marketing Date20210709
Marketing Category NameNDA
Application NumberNDA215341
ManufacturerBayer HealthCare Pharmaceuticals Inc.
Substance NameFINERENONE
Strength40
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/50419-542-02





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