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"70518-3477-1" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1)
(REMEDYREPACK INC.)
NDC Code
70518-3477-1
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1)
Product NDC
70518-3477
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
20220816
Marketing Category Name
ANDA
Application Number
ANDA209286
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/70518-3477-1