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"48792-7874-2" National Drug Code (NDC)

Rivaroxaban 90 TABLET, FILM COATED in 1 BOTTLE (48792-7874-2)
(Sunshine Lake Pharma Co.,Ltd.)

NDC Code48792-7874-2
Package Description90 TABLET, FILM COATED in 1 BOTTLE (48792-7874-2)
Product NDC48792-7874
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRivaroxaban
Non-Proprietary NameRivaroxaban
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250514
Marketing Category NameANDA
Application NumberANDA213348
ManufacturerSunshine Lake Pharma Co.,Ltd.
Substance NameRIVAROXABAN
Strength20
Strength Unitmg/1
Pharmacy ClassesFactor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7874-2





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