"33342-191-12" National Drug Code (NDC)

Amlodipine And Olmesartan Medoxomil 10 BLISTER PACK in 1 CARTON (33342-191-12) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Macleods Pharmaceuticals Limited)

NDC Code33342-191-12
Package Description10 BLISTER PACK in 1 CARTON (33342-191-12) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC33342-191
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine And Olmesartan Medoxomil
Non-Proprietary NameAmlodipine And Olmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20161027
Marketing Category NameANDA
Application NumberANDA206884
ManufacturerMacleods Pharmaceuticals Limited
Substance NameAMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength5; 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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