"68180-266-03" National Drug Code (NDC)

Divalproex Sodium 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-266-03)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-266-03
Package Description1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-266-03)
Product NDC68180-266
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20080729
Marketing Category NameANDA
Application NumberANDA078790
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameDIVALPROEX SODIUM
Strength250
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]

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