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"68180-261-02" National Drug Code (NDC)
Divalproex Sodium 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-261-02
Package Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02)
Product NDC
68180-261
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20200918
Marketing Category Name
ANDA
Application Number
ANDA209286
Manufacturer
Lupin Pharmaceuticals, 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/68180-261-02