"59651-457-99" National Drug Code (NDC)

Carbidopa And Levodopa 1000 TABLET in 1 BOTTLE (59651-457-99)
(Aurobindo Pharma Limited)

NDC Code59651-457-99
Package Description1000 TABLET in 1 BOTTLE (59651-457-99)
Product NDC59651-457
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarbidopa And Levodopa
Non-Proprietary NameCarbidopa And Levodopa
Dosage FormTABLET
UsageORAL
Start Marketing Date20221128
Marketing Category NameANDA
Application NumberANDA216537
ManufacturerAurobindo Pharma Limited
Substance NameCARBIDOPA; LEVODOPA
Strength25; 100
Strength Unitmg/1; mg/1
Pharmacy ClassesAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]

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