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"68071-4102-3" National Drug Code (NDC)

Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4102-3)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-4102-3
Package Description30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4102-3)
Product NDC68071-4102
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20111001
Marketing Category NameANDA
Application NumberANDA079163
ManufacturerNuCare Pharmaceuticals,Inc.
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/68071-4102-3





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