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"68382-315-05" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-315-05)
(Zydus Pharmaceuticals USA Inc)

NDC Code68382-315-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-315-05)
Product NDC68382-315
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Proprietary Name SuffixExtended Release
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20130812
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021168
ManufacturerZydus Pharmaceuticals USA 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/68382-315-05





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