"62756-796-13" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code62756-796-13
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-13)
Product NDC62756-796
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20080729
Marketing Category NameANDA
Application NumberANDA078597
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameDIVALPROEX SODIUM
Strength125
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]

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