www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"68788-7183-9" National Drug Code (NDC)

Divalproex Sodium 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-9)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7183-9
Package Description90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-9)
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/68788-7183-9





Copyright © 2007-2024 www.ndcvalidator.com