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"50419-540-02" National Drug Code (NDC)
Kerendia 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-540-02)
(Bayer Healthcare Pharmaceuticals Inc.)
NDC Code
50419-540-02
Package Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-540-02)
Product NDC
50419-540
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Kerendia
Non-Proprietary Name
Finerenone
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210709
Marketing Category Name
NDA
Application Number
NDA215341
Manufacturer
Bayer Healthcare Pharmaceuticals Inc.
Substance Name
FINERENONE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Mineralocorticoid Receptor Antagonists [MoA], Nonsteroidal Mineralocorticoid-Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50419-540-02