"70518-1902-1" National Drug Code (NDC)

Pravastatin Sodium 30 TABLET in 1 BLISTER PACK (70518-1902-1)
(REMEDYREPACK INC.)

NDC Code70518-1902-1
Package Description30 TABLET in 1 BLISTER PACK (70518-1902-1)
Product NDC70518-1902
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePravastatin Sodium
Non-Proprietary NamePravastatin Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20190222
Marketing Category NameANDA
Application NumberANDA207068
ManufacturerREMEDYREPACK INC.
Substance NamePRAVASTATIN SODIUM
Strength40
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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