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"49349-822-02" National Drug Code (NDC)

Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-822-02)
(REMEDYREPACK INC.)

NDC Code49349-822-02
Package Description30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-822-02)
Product NDC49349-822
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20111130
Marketing Category NameANDA
Application NumberANDA078597
ManufacturerREMEDYREPACK INC.
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/49349-822-02





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