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"58118-0797-3" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BOTTLE (58118-0797-3)
(Clinical Solutions Wholesale)
NDC Code
58118-0797-3
Package Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (58118-0797-3)
Product NDC
58118-0797
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20080729
Marketing Category Name
ANDA
Application Number
ANDA078597
Manufacturer
Clinical Solutions Wholesale
Substance Name
DIVALPROEX SODIUM
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Anti-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/58118-0797-3