0115-1460 : Fenofibric Acid 135 mg Delayed Release Capsule

NDC:	0115-1460
Labeler:	Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type:	Human Prescription Drug
Drug Name:	Fenofibric Acid
Dosage Form:	Oral Capsule, Delayed Release
Application #:	NDA022224
Rev. Date:	Dec 15, 2008

Appearance:

Markings:	135;a
Shapes:	Capsule
Colors:	Blue / Yellow
Size (mm):	22
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

135 a: (0115-1460) Fenofibric Acid 135 mg Delayed Release Capsule by Global Pharmaceuticals, Division of Impax Laboratories Inc.

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

0115-1460-10: 90 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (0115‑1460‑10)

Active Ingredients:

Fenofibric Acid

Dosage Strength:

135 mg

Pharmaceutical Classes:

Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC QR Code

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NDC 0115-1460 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.