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"69452-435-20" National Drug Code (NDC)
Divalproex Sodium 100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-20)
(Bionpharma Inc.)
NDC Code
69452-435-20
Package Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-20)
Product NDC
69452-435
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20240626
Marketing Category Name
ANDA
Application Number
ANDA078853
Manufacturer
Bionpharma 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/69452-435-20