www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"68071-4102-6" National Drug Code (NDC)
Divalproex Sodium 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4102-6)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-4102-6
Package Description
60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4102-6)
Product NDC
68071-4102
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
20111001
Marketing Category Name
ANDA
Application Number
ANDA079163
Manufacturer
NuCare Pharmaceuticals,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/68071-4102-6