"70771-1459-9" National Drug Code (NDC)

Amlodipine And Atorvastatin 90 TABLET, FILM COATED in 1 BOTTLE (70771-1459-9)
(Zydus Lifesciences Limited)

NDC Code70771-1459-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (70771-1459-9)
Product NDC70771-1459
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine And Atorvastatin
Non-Proprietary NameAmlodipine And Atorvastatin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190530
Marketing Category NameANDA
Application NumberANDA207762
ManufacturerZydus Lifesciences Limited
Substance NameAMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
Strength2.5; 40
Strength Unitmg/1; mg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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