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"49349-072-02" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-072-02)
(REMEDYREPACK INC.)
NDC Code
49349-072-02
Package Description
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-072-02)
Product NDC
49349-072
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Proprietary Name Suffix
Delayed Release
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20101116
Marketing Category Name
ANDA
Application Number
ANDA076941
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/49349-072-02