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"55111-332-10" National Drug Code (NDC)

Pantoprazole 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-10)
(Dr.Reddy's Laboratories Limited)

NDC Code55111-332-10
Package Description1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-10)
Product NDC55111-332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePantoprazole
Non-Proprietary NamePantoprazole
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20110119
Marketing Category NameANDA
Application NumberANDA077619
ManufacturerDr.Reddy's Laboratories Limited
Substance NamePANTOPRAZOLE 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/55111-332-10





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