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"69844-023-03" National Drug Code (NDC)
Fenofibric Acid Delayed-release 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69844-023-03)
(Graviti Pharmaceuticals Private Limited)
NDC Code
69844-023-03
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69844-023-03)
Product NDC
69844-023
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibric Acid Delayed-release
Non-Proprietary Name
Fenofibric Acid
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20190718
Marketing Category Name
ANDA
Application Number
ANDA211626
Manufacturer
Graviti Pharmaceuticals Private Limited
Substance Name
FENOFIBRIC ACID
Strength
135
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69844-023-03