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"70518-2033-0" National Drug Code (NDC)
Divalproex Sodium 100 POUCH in 1 BOX (70518-2033-0) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-2033-1)
(REMEDYREPACK INC.)
NDC Code
70518-2033-0
Package Description
100 POUCH in 1 BOX (70518-2033-0) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-2033-1)
Product NDC
70518-2033
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
20190422
Marketing Category Name
ANDA
Application Number
ANDA078239
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/70518-2033-0