"65841-637-05" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-637-05)
(Zydus Lifesciences Limited)

NDC Code65841-637-05
Package Description500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-637-05)
Product NDC65841-637
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20130107
Marketing Category NameANDA
Application NumberANDA078239
ManufacturerZydus Lifesciences Limited
Substance NameDIVALPROEX SODIUM
Strength250
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]

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