"0615-7531-31" National Drug Code (NDC)

Divalproex Sodium 31 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7531-31)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-7531-31
Package Description31 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7531-31)
Product NDC0615-7531
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
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
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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