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"68180-267-02" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-267-02)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-267-02
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-267-02)
Product NDC68180-267
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20080729
Marketing Category NameANDA
Application NumberANDA078790
ManufacturerLupin Pharmaceuticals, 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/68180-267-02





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