"0093-9703-05" National Drug Code (NDC)

Carbidopa And Levodopa 500 TABLET in 1 BOTTLE (0093-9703-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-9703-05
Package Description500 TABLET in 1 BOTTLE (0093-9703-05)
Product NDC0093-9703
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarbidopa And Levodopa
Non-Proprietary NameCarbidopa And Levodopa
Dosage FormTABLET
UsageORAL
Start Marketing Date20231215
Marketing Category NameANDA
Application NumberANDA074260
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameCARBIDOPA; LEVODOPA
Strength25; 250
Strength Unitmg/1; mg/1
Pharmacy ClassesAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]

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