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"70934-949-60" National Drug Code (NDC)

Divalproex Sodium 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-949-60)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-949-60
Package Description60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-949-60)
Product NDC70934-949
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20220209
End Marketing Date20240630
Marketing Category NameANDA
Application NumberANDA079163
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
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/70934-949-60





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