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"65862-959-01" National Drug Code (NDC)
Divalproex Sodium 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-01)
(Aurobindo Pharma Limited)
NDC Code
65862-959-01
Package Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-01)
Product NDC
65862-959
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
20141024
Marketing Category Name
ANDA
Application Number
ANDA090554
Manufacturer
Aurobindo Pharma Limited
Substance Name
DIVALPROEX SODIUM
Strength
125
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/65862-959-01