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"55648-725-03" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-725-03)
(WOCKHARDT LIMITED)

NDC Code55648-725-03
Package Description500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-725-03)
Product NDC55648-725
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Proprietary Name SuffixEr
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20090804
Marketing Category NameANDA
Application NumberANDA078705
ManufacturerWOCKHARDT LIMITED
Substance NameDIVALPROEX SODIUM
Strength500
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/55648-725-03





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