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"37835-001-42" National Drug Code (NDC)

Omeprazole 3 BOTTLE in 1 CARTON (37835-001-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
(BI-MART)

NDC Code37835-001-42
Package Description3 BOTTLE in 1 CARTON (37835-001-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC37835-001
Product Type NameHUMAN OTC DRUG
Proprietary NameOmeprazole
Non-Proprietary NameOmeprazole
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20190930
Marketing Category NameANDA
Application NumberANDA207891
ManufacturerBI-MART
Substance NameOMEPRAZOLE
Strength20
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37835-001-42





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