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"37808-569-45" National Drug Code (NDC)
Omeprazole Delayed-release 1 BOTTLE in 1 CARTON (37808-569-45) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
(H-E-B)
NDC Code
37808-569-45
Package Description
1 BOTTLE in 1 CARTON (37808-569-45) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC
37808-569
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Omeprazole Delayed-release
Non-Proprietary Name
Omeprazole
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20260701
Marketing Category Name
ANDA
Application Number
ANDA218829
Manufacturer
H-E-B
Substance Name
OMEPRAZOLE MAGNESIUM
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/37808-569-45