"70518-1905-0" National Drug Code (NDC)

Crestor 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1905-0)
(REMEDYREPACK INC.)

NDC Code70518-1905-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1905-0)
Product NDC70518-1905
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCrestor
Non-Proprietary NameRosuvastatin Calcium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190225
Marketing Category NameNDA
Application NumberNDA021366
ManufacturerREMEDYREPACK INC.
Substance NameROSUVASTATIN CALCIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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