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"0781-2243-01" National Drug Code (NDC)
Divalproex Sodium 100 CAPSULE in 1 BOTTLE (0781-2243-01)
(Sandoz Inc.)
NDC Code
0781-2243-01
Package Description
100 CAPSULE in 1 BOTTLE (0781-2243-01)
Product NDC
0781-2243
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Proprietary Name Suffix
Delayed Release (sprinkle)
Non-Proprietary Name
Divalproex Sodium
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20150831
End Marketing Date
20211105
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA019680
Manufacturer
Sandoz Inc.
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/0781-2243-01