"70710-1721-1" National Drug Code (NDC)

Carbidopa And Levodopa 100 TABLET in 1 BOTTLE (70710-1721-1)
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1721-1
Package Description100 TABLET in 1 BOTTLE (70710-1721-1)
Product NDC70710-1721
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarbidopa And Levodopa
Non-Proprietary NameCarbidopa And Levodopa
Dosage FormTABLET
UsageORAL
Start Marketing Date20240824
Marketing Category NameANDA
Application NumberANDA215999
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameCARBIDOPA; LEVODOPA
Strength10; 100
Strength Unitmg/1; mg/1
Pharmacy ClassesAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]

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