"33342-175-12" National Drug Code (NDC)

Olmesartan Medoxomil And Hydrochlorothiazide 10 BLISTER PACK in 1 CARTON (33342-175-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Macleods Pharmaceuticals Limited)

NDC Code33342-175-12
Package Description10 BLISTER PACK in 1 CARTON (33342-175-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC33342-175
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil And Hydrochlorothiazide
Non-Proprietary NameOlmesartan Medoxomil And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230602
Marketing Category NameANDA
Application NumberANDA204801
ManufacturerMacleods Pharmaceuticals Limited
Substance NameHYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength25; 40
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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