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"60687-879-61" National Drug Code (NDC)

Divalproex Sodium 90 BLISTER PACK in 1 CARTON (60687-879-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-879-11)
(American Health Packaging)

NDC Code60687-879-61
Package Description90 BLISTER PACK in 1 CARTON (60687-879-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-879-11)
Product NDC60687-879
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20250110
Marketing Category NameANDA
Application NumberANDA079163
ManufacturerAmerican Health Packaging
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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