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"70710-1072-1" National Drug Code (NDC)

Modafinil 100 TABLET in 1 BOTTLE (70710-1072-1)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code70710-1072-1
Package Description100 TABLET in 1 BOTTLE (70710-1072-1)
Product NDC70710-1072
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameModafinil
Non-Proprietary NameModafinil
Dosage FormTABLET
UsageORAL
Start Marketing Date20180104
Marketing Category NameANDA
Application NumberANDA209966
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameMODAFINIL
Strength100
Strength Unitmg/1
Pharmacy ClassesCentral Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC]
DEA ScheduleCIV

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-1072-1





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