"51138-211-30" National Drug Code (NDC)

Benicar 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-211-30)
(Med-Health Pharma, LLC)

NDC Code51138-211-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-211-30)
Product NDC51138-211
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenicar
Non-Proprietary NameOlmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120202
Marketing Category NameNDA
Application NumberNDA021286
ManufacturerMed-Health Pharma, LLC
Substance NameOLMESARTAN MEDOXOMIL
Strength5
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

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