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"68001-105-00" National Drug Code (NDC)

Divalproex Sodium 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-00)
(BluePoint Laboratories)

NDC Code68001-105-00
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-00)
Product NDC68001-105
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20131008
Marketing Category NameANDA
Application NumberANDA078239
ManufacturerBluePoint Laboratories
Substance NameDIVALPROEX SODIUM
Strength250
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/68001-105-00





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