"60505-3492-3" National Drug Code (NDC)

Amlodipine And Atorvastatin 30 TABLET, FILM COATED in 1 BOTTLE (60505-3492-3)
(Apotex Corp.)

NDC Code60505-3492-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (60505-3492-3)
Product NDC60505-3492
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine And Atorvastatin
Non-Proprietary NameAmlodipine And Atorvastatin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200729
Marketing Category NameANDA
Application NumberANDA205199
ManufacturerApotex Corp.
Substance NameAMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
Strength5; 80
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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