Drugplain

FENOFIBRIC ACID DELAYED-RELEASE 45 mg/1

FENOFIBRIC ACID · CAPSULE, DELAYED RELEASE · Laurus Labs Limited

No Recall History
Plain English

FENOFIBRIC ACID DELAYED-RELEASE is a capsule, delayed release containing fenofibric acid at 45 mg/1, taken oral. Manufactured by Laurus Labs Limited.

Key Facts

Brand Name
FENOFIBRIC ACID DELAYED-RELEASE
Generic Name
FENOFIBRIC ACID
NDC Code (Product)
42385-944
Manufacturer
Laurus Labs Limited
Strength
45 mg/1
Dosage Form
CAPSULE, DELAYED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA211626
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Marketing Start
08/24/2020

Recall History

No Recall History

Frequently Asked Questions

What is FENOFIBRIC ACID DELAYED-RELEASE used for?

FENOFIBRIC ACID DELAYED-RELEASE contains FENOFIBRIC ACID. It is a capsule, delayed release taken oral. Consult your doctor for specific uses.

Is FENOFIBRIC ACID DELAYED-RELEASE a controlled substance?

FENOFIBRIC ACID DELAYED-RELEASE is not classified as a controlled substance by the DEA.

What is the generic name for FENOFIBRIC ACID DELAYED-RELEASE?

The generic name for FENOFIBRIC ACID DELAYED-RELEASE is FENOFIBRIC ACID. There are 10 other brand versions of FENOFIBRIC ACID.

What is the NDC code for FENOFIBRIC ACID DELAYED-RELEASE 45 mg/1?

The NDC (National Drug Code) for FENOFIBRIC ACID DELAYED-RELEASE 45 mg/1 is 42385-944, listed by Laurus Labs Limited.