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"61786-175-02" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (61786-175-02)
(REMEDYREPACK INC.)
NDC Code
61786-175-02
Package Description
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (61786-175-02)
Product NDC
61786-175
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
20150217
Marketing Category Name
ANDA
Application Number
ANDA079163
Manufacturer
REMEDYREPACK 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/61786-175-02