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"37835-001-14" National Drug Code (NDC)
Omeprazole 1 BOTTLE in 1 CARTON (37835-001-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
(BI-MART)
NDC Code
37835-001-14
Package Description
1 BOTTLE in 1 CARTON (37835-001-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC
37835-001
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Omeprazole
Non-Proprietary Name
Omeprazole
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20190930
Marketing Category Name
ANDA
Application Number
ANDA207891
Manufacturer
BI-MART
Substance Name
OMEPRAZOLE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37835-001-14