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"68001-441-39" National Drug Code (NDC)
Omeprazole 2 BOTTLE in 1 CARTON (68001-441-39) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)
(BluePoint Laboratories)
NDC Code
68001-441-39
Package Description
2 BOTTLE in 1 CARTON (68001-441-39) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)
Product NDC
68001-441
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Omeprazole
Non-Proprietary Name
Omeprazole
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20200619
Marketing Category Name
ANDA
Application Number
ANDA207740
Manufacturer
BluePoint Laboratories
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/68001-441-39