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"55111-532-78" National Drug Code (NDC)

Divalproex Sodium 10 BLISTER PACK in 1 CARTON (55111-532-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-532-79)
(Dr. Reddy's Laboratories Ltd)

NDC Code55111-532-78
Package Description10 BLISTER PACK in 1 CARTON (55111-532-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-532-79)
Product NDC55111-532
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20090123
Marketing Category NameANDA
Application NumberANDA078979
ManufacturerDr. Reddy's Laboratories Ltd
Substance NameDIVALPROEX SODIUM
Strength125
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]

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