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"0832-7124-01" National Drug Code (NDC)
Divalproex Sodium 100 BLISTER PACK in 1 CARTON (0832-7124-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0832-7124-89)
(Upsher-Smith Laboratories, LLC)
NDC Code
0832-7124-01
Package Description
100 BLISTER PACK in 1 CARTON (0832-7124-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0832-7124-89)
Product NDC
0832-7124
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
20140321
Marketing Category Name
ANDA
Application Number
ANDA078182
Manufacturer
Upsher-Smith Laboratories, LLC
Substance Name
DIVALPROEX SODIUM
Strength
500
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/0832-7124-01