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"48792-7878-1" National Drug Code (NDC)

Olmesartan Medoxomil 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7878-1)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7878-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7878-1)
Product NDC48792-7878
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil
Non-Proprietary NameOlmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190305
Marketing Category NameANDA
Application NumberANDA211049
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameOLMESARTAN MEDOXOMIL
Strength20
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7878-1





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