"68180-261-02" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-261-02
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02)
Product NDC68180-261
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200918
Marketing Category NameANDA
Application NumberANDA209286
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]

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