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"0093-7440-01" National Drug Code (NDC)
Divalproex Sodium 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-7440-01)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-7440-01
Package Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-7440-01)
Product NDC
0093-7440
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
End Marketing Date
20190630
Marketing Category Name
ANDA
Application Number
ANDA076941
Manufacturer
Teva Pharmaceuticals USA, 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/0093-7440-01