"61919-648-30" National Drug Code (NDC)

Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-648-30)
(DIRECT RX)

NDC Code61919-648-30
Package Description30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-648-30)
Product NDC61919-648
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA078597
ManufacturerDIRECT RX
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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