"68462-567-90" National Drug Code (NDC)

Amlodipine And Olmesartan Medoxomil 90 TABLET, FILM COATED in 1 BOTTLE (68462-567-90)
(Glenmark Pharmaceuticals Inc., USA)

NDC Code68462-567-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68462-567-90)
Product NDC68462-567
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine And Olmesartan Medoxomil
Non-Proprietary NameAmlodipine And Olmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170705
Marketing Category NameANDA
Application NumberANDA207807
ManufacturerGlenmark Pharmaceuticals Inc., USA
Substance NameAMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength10; 20
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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