"67877-502-90" National Drug Code (NDC)

Amlodipine And Olmesartan Medoxomil 90 TABLET in 1 BOTTLE (67877-502-90)
(Ascend Laboratories, LLC)

NDC Code67877-502-90
Package Description90 TABLET in 1 BOTTLE (67877-502-90)
Product NDC67877-502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine And Olmesartan Medoxomil
Non-Proprietary NameAmlodipine And Olmesartan Medoxomil
Dosage FormTABLET
UsageORAL
Start Marketing Date20170814
Marketing Category NameANDA
Application NumberANDA209042
ManufacturerAscend Laboratories, LLC
Substance NameAMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength10; 40
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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