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"68084-782-33" National Drug Code (NDC)

Divalproex Sodium 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-33)
(American Health Packaging)

NDC Code68084-782-33
Package Description1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-33)
Product NDC68084-782
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20141007
Marketing Category NameANDA
Application NumberANDA090554
ManufacturerAmerican Health Packaging
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/68084-782-33





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