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"16714-512-02" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (16714-512-02)
(Northstar Rx LLC)

NDC Code16714-512-02
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (16714-512-02)
Product NDC16714-512
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20090714
End Marketing Date20140831
Marketing Category NameANDA
Application NumberANDA078853
ManufacturerNorthstar Rx LLC
Substance NameDIVALPROEX SODIUM
Strength250
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/16714-512-02





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