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"68382-031-05" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-031-05)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-031-05
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-031-05)
Product NDC68382-031
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20100306
Marketing Category NameANDA
Application NumberANDA077100
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameDIVALPROEX SODIUM
Strength125
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/68382-031-05





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