"60290-067-02" National Drug Code (NDC)

Oxcarbazepine 500 TABLET, FILM COATED in 1 BOTTLE (60290-067-02)
(Umedica Laboratories USA Inc.)

NDC Code60290-067-02
Package Description500 TABLET, FILM COATED in 1 BOTTLE (60290-067-02)
Product NDC60290-067
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxcarbazepine
Non-Proprietary NameOxcarbazepine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260101
Marketing Category NameANDA
Application NumberANDA218341
ManufacturerUmedica Laboratories USA Inc.
Substance NameOXCARBAZEPINE
Strength150
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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