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"51991-683-10" National Drug Code (NDC)

Rabeprazole Sodium 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (51991-683-10)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-683-10
Package Description1000 TABLET, DELAYED RELEASE in 1 BOTTLE (51991-683-10)
Product NDC51991-683
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRabeprazole Sodium
Non-Proprietary NameRabeprazole Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20170601
End Marketing Date20200228
Marketing Category NameANDA
Application NumberANDA204237
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameRABEPRAZOLE SODIUM
Strength20
Strength Unitmg/1
Pharmacy ClassesProton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51991-683-10





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