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"51672-4139-0" National Drug Code (NDC)
Lamotrigine 10 BLISTER PACK in 1 CARTON (51672-4139-0) > 10 TABLET, CHEWABLE in 1 BLISTER PACK
(Taro Pharmaceuticals U.S.A., Inc.)
NDC Code
51672-4139-0
Package Description
10 BLISTER PACK in 1 CARTON (51672-4139-0) > 10 TABLET, CHEWABLE in 1 BLISTER PACK
Product NDC
51672-4139
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lamotrigine
Non-Proprietary Name
Lamotrigine
Dosage Form
TABLET, CHEWABLE
Usage
ORAL
Start Marketing Date
20090204
Marketing Category Name
ANDA
Application Number
ANDA079204
Manufacturer
Taro Pharmaceuticals U.S.A., Inc.
Substance Name
LAMOTRIGINE
Strength
5
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/51672-4139-0