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"65862-594-01" National Drug Code (NDC)
Divalproex Sodium 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)
(Aurobindo Pharma Limited)
NDC Code
65862-594-01
Package Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)
Product NDC
65862-594
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20140602
Marketing Category Name
ANDA
Application Number
ANDA202419
Manufacturer
Aurobindo Pharma Limited
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/65862-594-01