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"0245-0182-15" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0245-0182-15)
(Upsher-Smith Laboratories, Inc.)

NDC Code0245-0182-15
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (0245-0182-15)
Product NDC0245-0182
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
ManufacturerUpsher-Smith Laboratories, Inc.
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/0245-0182-15





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