"60722-5011-1" National Drug Code (NDC)

Prednisolone 1000 TABLET in 1 BOTTLE (60722-5011-1)
(Zhejiang Xianju Pharmaceutical Co., Ltd.)

NDC Code60722-5011-1
Package Description1000 TABLET in 1 BOTTLE (60722-5011-1)
Product NDC60722-5011
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisolone
Non-Proprietary NamePrednisolone
Dosage FormTABLET
UsageORAL
Start Marketing Date20240901
Marketing Category NameANDA
Application NumberANDA218083
ManufacturerZhejiang Xianju Pharmaceutical Co., Ltd.
Substance NamePREDNISOLONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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