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"51991-772-10" National Drug Code (NDC)

Lansoprazole 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51991-772-10)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-772-10
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51991-772-10)
Product NDC51991-772
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLansoprazole
Non-Proprietary NameLansoprazole
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20121218
End Marketing Date20210531
Marketing Category NameANDA
Application NumberANDA201921
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameLANSOPRAZOLE
Strength30
Strength Unitmg/1
Pharmacy ClassesProton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51991-772-10





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