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"68001-472-03" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03)
(BluePoint Laboratories)

NDC Code68001-472-03
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03)
Product NDC68001-472
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20210120
Marketing Category NameANDA
Application NumberANDA079163
ManufacturerBluePoint Laboratories
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/68001-472-03





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