"68151-4162-7" National Drug Code (NDC)

Divalproex Sodium 1 TABLET, DELAYED RELEASE in 1 CUP, UNIT-DOSE (68151-4162-7)
(Carilion Materials Management)

NDC Code68151-4162-7
Package Description1 TABLET, DELAYED RELEASE in 1 CUP, UNIT-DOSE (68151-4162-7)
Product NDC68151-4162
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
ManufacturerCarilion Materials Management
Substance NameDIVALPROEX SODIUM
Strength500
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

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