"70518-1322-2" National Drug Code (NDC)

Atorvastatin Calcium 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1322-2)
(REMEDYREPACK INC.)

NDC Code70518-1322-2
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1322-2)
Product NDC70518-1322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtorvastatin Calcium
Non-Proprietary NameAtorvastatin Calcium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180725
Marketing Category NameANDA
Application NumberANDA090548
ManufacturerREMEDYREPACK INC.
Substance NameATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
Strength40
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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