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"48792-7873-1" National Drug Code (NDC)

Rivaroxaban 30 TABLET, FILM COATED in 1 BOTTLE (48792-7873-1)
(Sunshine Lake Pharma Co.,Ltd.)

NDC Code48792-7873-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (48792-7873-1)
Product NDC48792-7873
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
Strength15
Strength Unitmg/1
Pharmacy ClassesFactor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7873-1





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