"70518-2647-0" National Drug Code (NDC)

Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide 40/5/25 Mg 30 TABLET in 1 BOTTLE, PLASTIC (70518-2647-0)
(REMEDYREPACK INC.)

NDC Code70518-2647-0
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70518-2647-0)
Product NDC70518-2647
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide 40/5/25 Mg
Non-Proprietary NameOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide Tablet 40/5/25 Mg
Dosage FormTABLET
UsageORAL
Start Marketing Date20200324
Marketing Category NameANDA
Application NumberANDA203580
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength5; 25; 40
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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