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"55111-530-30" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-530-30)
(Dr.Reddy's Laboratories Limited)
NDC Code
55111-530-30
Package Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-530-30)
Product NDC
55111-530
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
ANDA078755
Manufacturer
Dr.Reddy's Laboratories 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/55111-530-30