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"70518-0282-0" National Drug Code (NDC)

Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-0282-0)
(REMEDYREPACK INC.)

NDC Code70518-0282-0
Package Description30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-0282-0)
Product NDC70518-0282
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20170303
Marketing Category NameANDA
Application NumberANDA079163
ManufacturerREMEDYREPACK 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/70518-0282-0





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