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"0093-7441-05" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-7441-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7441-05
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-7441-05)
Product NDC0093-7441
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20080729
End Marketing Date20190930
Marketing Category NameANDA
Application NumberANDA076941
ManufacturerTeva 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/0093-7441-05





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