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"62756-796-13" National Drug Code (NDC)
Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-13)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
62756-796-13
Package Description
500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-13)
Product NDC
62756-796
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
ANDA078597
Manufacturer
Sun Pharmaceutical Industries, 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/62756-796-13