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"61919-176-72" National Drug Code (NDC)
Omeprazole Dr 120 BOTTLE in 1 BOTTLE (61919-176-72) > 90 BOTTLE in 1 BOTTLE (61919-176-90) > 60 BOTTLE in 1 BOTTLE (61919-176-60) > 30 BOTTLE in 1 BOTTLE (61919-176-30) > 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (61919-176-15)
(Direct Rx)
NDC Code
61919-176-72
Package Description
120 BOTTLE in 1 BOTTLE (61919-176-72) > 90 BOTTLE in 1 BOTTLE (61919-176-90) > 60 BOTTLE in 1 BOTTLE (61919-176-60) > 30 BOTTLE in 1 BOTTLE (61919-176-30) > 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (61919-176-15)
Product NDC
61919-176
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Omeprazole Dr
Non-Proprietary Name
Omeprazole Dr
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20150101
Marketing Category Name
ANDA
Application Number
ANDA076048
Manufacturer
Direct Rx
Substance Name
OMEPRAZOLE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-176-72