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"51991-294-05" National Drug Code (NDC)

Oxcarbazepine 500 TABLET, FILM COATED in 1 BOTTLE (51991-294-05)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-294-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (51991-294-05)
Product NDC51991-294
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxcarbazepine
Non-Proprietary NameOxcarbazepine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20080111
Marketing Category NameANDA
Application NumberANDA078069
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameOXCARBAZEPINE
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51991-294-05





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