"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 Code61919-176-72
Package Description120 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 NDC61919-176
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOmeprazole Dr
Non-Proprietary NameOmeprazole Dr
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA076048
ManufacturerDirect Rx
Substance NameOMEPRAZOLE
Strength20
Strength Unitmg/1
Pharmacy ClassesProton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]

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