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"55111-531-78" National Drug Code (NDC)

Divalproex Sodium 10 BLISTER PACK in 1 CARTON (55111-531-78) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)
(Dr.Reddy's Laboratories Limited)

NDC Code55111-531-78
Package Description10 BLISTER PACK in 1 CARTON (55111-531-78) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)
Product NDC55111-531
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20080729
Marketing Category NameANDA
Application NumberANDA078755
ManufacturerDr.Reddy's Laboratories 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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