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"0245-0181-15" National Drug Code (NDC)
Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0245-0181-15)
(Upsher-Smith Laboratories, Inc.)
NDC Code
0245-0181-15
Package Description
500 TABLET, DELAYED RELEASE in 1 BOTTLE (0245-0181-15)
Product NDC
0245-0181
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
20110121
Marketing Category Name
ANDA
Application Number
ANDA078182
Manufacturer
Upsher-Smith Laboratories, Inc.
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/0245-0181-15