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"0245-0182-01" National Drug Code (NDC)

Divalproex Sodium 10 BLISTER PACK in 1 CARTON (0245-0182-01) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0245-0182-89)
(Upsher-Smith Laboratories, Inc.)

NDC Code0245-0182-01
Package Description10 BLISTER PACK in 1 CARTON (0245-0182-01) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0245-0182-89)
Product NDC0245-0182
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20110121
Marketing Category NameANDA
Application NumberANDA078182
ManufacturerUpsher-Smith Laboratories, Inc.
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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