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"55648-725-04" National Drug Code (NDC)

Divalproex Sodium 10 BLISTER PACK in 1 CARTON (55648-725-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
(WOCKHARDT LIMITED)

NDC Code55648-725-04
Package Description10 BLISTER PACK in 1 CARTON (55648-725-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
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]

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