0074-3161 : Trilipix 45 mg Oral Capsule, Delayed Release


NDC: 0074-3161
Labeler: Abbvie Inc.
Product Type: Human Prescription Drug
Drug Name:  Trilipix
Dosage Form: Oral Capsule, Delayed Release
Application #: NDA022224
Rev. Date: 


Appearance:


Markings: 45
Shapes:  Capsule
Colors:  Yellow / Red
Size (mm): 16
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.

NDC Package Codes:

  • 0074-3161-90: 90 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (0074‑3161‑90)

Active Ingredients:

  • Fenofibric Acid

Dosage Strength:

  • 45 mg

Inactive Ingredients:

  • Hydroxypropyl Cellulose (Type H)
  • Ferric Oxide Yellow
  • Ferrosoferric Oxide
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Povidones
  • Hypromelloses
  • Ferric Oxide Red
  • Titanium Dioxide
  • Gelatin
  • Triethyl Citrate
  • Talc
  • Sodium Stearyl Fumarate
  • Silicon Dioxide
  • Water

Pharmaceutical Classes:

  • Peroxisome Proliferator Receptor alpha Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0074-3162 Trilipix 135 mg Oral Capsule, Delayed Release by Abbvie Inc.
  • 0074-9189 Trilipix 135 mg Enteric Coated Capsule 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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NDC 0074-3161 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.