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"70518-0312-0" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0312-0)
(REMEDYREPACK INC.)
NDC Code
70518-0312-0
Package Description
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0312-0)
Product NDC
70518-0312
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20170313
Marketing Category Name
ANDA
Application Number
ANDA090161
Manufacturer
REMEDYREPACK INC.
Substance Name
DIVALPROEX SODIUM
Strength
250
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/70518-0312-0