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"0615-7850-39" National Drug Code (NDC)

Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7850-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-7850-39
Package Description30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7850-39)
Product NDC0615-7850
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20100306
Marketing Category NameANDA
Application NumberANDA077100
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameDIVALPROEX SODIUM
Strength500
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0615-7850-39





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