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"67296-1635-1" National Drug Code (NDC)
Divalproex Sodium 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-1635-1)
(RedPharm Drug, Inc.)
NDC Code
67296-1635-1
Package Description
10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-1635-1)
Product NDC
67296-1635
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
20190101
Marketing Category Name
ANDA
Application Number
ANDA078791
Manufacturer
RedPharm Drug, 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/67296-1635-1