www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"68180-266-02" National Drug Code (NDC)
Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-266-02)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-266-02
Package Description
500 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-266-02)
Product NDC
68180-266
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
20080729
Marketing Category Name
ANDA
Application Number
ANDA078790
Manufacturer
Lupin 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/68180-266-02