0074-9189 : Trilipix 135 mg Enteric Coated Capsule


NDC0074-9189
Labeler: Abbvie Inc.
Product Type: Human Prescription Drug
Drug Name:  Trilipix
Dosage Form: Oral Capsule, Delayed Release
Application #: NDA022224
Rev. Date: 


Appearance:


Markings: a;135
Shapes:  Capsule
Colors:  Yellow / Blue
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.

a 135: (0074-9189) Trilipix 135 mg Enteric Coated Capsule by Abbvie 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:

  • 0074-9189-07: 1 BLISTER PACK IN 1 CARTON (0074‑9189‑07) > 7 CAPSULE, DELAYED RELEASE IN 1 BLISTER PACK
  • 0074-9189-10: 5 BLISTER PACK IN 1 CARTON (0074‑9189‑10) > 6 CAPSULE, DELAYED RELEASE IN 1 BLISTER PACK
  • 0074-9189-90: 90 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (0074‑9189‑90)

Active Ingredients:

  • Fenofibric Acid

Dosage Strength:

  • 135 mg

Inactive Ingredients:

  • Methacrylic Acid
  • Hydroxypropyl Cellulose (Type H)

Pharmaceutical Classes:

  • Peroxisome Proliferator Receptor alpha Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0074-3161 Trilipix 45 mg Oral Capsule, Delayed Release by Abbvie Inc.
  • 0074-3162 Trilipix 135 mg Oral Capsule, Delayed Release by Abbvie Inc.
  • 0074-9642 Trilipix 45 mg Enteric Coated Capsule by Abbvie Inc.
  • 54868-5986 Trilipix 135 mg Enteric Coated Capsule by Physicians Total Care, Inc.

NDC 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.