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"68180-363-13" National Drug Code (NDC)
Fenofibrate 10 BLISTER PACK in 1 CARTON (68180-363-13) > 10 TABLET in 1 BLISTER PACK (68180-363-11)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-363-13
Package Description
10 BLISTER PACK in 1 CARTON (68180-363-13) > 10 TABLET in 1 BLISTER PACK (68180-363-11)
Product NDC
68180-363
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20151123
End Marketing Date
20220531
Marketing Category Name
ANDA
Application Number
ANDA204019
Manufacturer
Lupin Pharmaceuticals, Inc.
Substance Name
FENOFIBRATE
Strength
160
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68180-363-13