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"61786-019-02" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (61786-019-02)
(REMEDYREPACK INC.)
NDC Code
61786-019-02
Package Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (61786-019-02)
Product NDC
61786-019
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20140902
Marketing Category Name
ANDA
Application Number
ANDA202419
Manufacturer
REMEDYREPACK INC.
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/61786-019-02