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"68788-7183-6" National Drug Code (NDC)

Divalproex Sodium 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-6)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7183-6
Package Description60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-6)
Product NDC68788-7183
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20180717
Marketing Category NameANDA
Application NumberANDA079163
ManufacturerPreferred Pharmaceuticals Inc.
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/68788-7183-6





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