68084-715 : Fenofibric Acid 135 mg Oral Capsule, Delayed Release

Labeler: American Health Packaging
Product Type: Human Prescription Drug
Drug Name:  Fenofibric Acid Delayed-release
Dosage Form: Oral Capsule, Delayed Release
Application #: ANDA201573
Rev. Date: 


Markings: C210;Par
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.

NDC Package Codes:

  • 68084-715-32: 20 BLISTER PACK IN 1 BOX, UNIT‑DOSE (68084‑715‑32) > 1 CAPSULE, DELAYED RELEASE IN 1 BLISTER PACK (68084‑715‑33)

Active Ingredients:

  • Choline Fenofibrate

Dosage Strength:

  • 135 mg

Inactive Ingredients:

  • Hydroxypropyl Cellulose (Type M)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Stearic Acid
  • Talc
  • Triethyl Citrate
  • Fd&c Blue No. 1
  • Fd&c Blue No. 2
  • Fd&c Red No. 40
  • D&c Yellow No. 10
  • Ferrosoferric Oxide
  • Propylene Glycol
  • Shellac
  • Fd&c Yellow No. 6
  • Gelatin
  • Titanium Dioxide

Pharmaceutical Classes:

  • Peroxisome Proliferator Receptor alpha Agonist [EPC]
  • Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
  • PPAR alpha [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 60429-432 Fenofibric Acid 135 mg Oral Capsule, Delayed Release by Golden State Medical Supply, Inc.
  • 69844-022 Fenofibric Acid Delayed-release Delayed-release 45 mg Oral Capsule, Delayed Release by Graviti Pharmaceuticals Private Limited
  • 69844-023 Fenofibric Acid Delayed-release Delayed-release 135 mg Oral Capsule, Delayed Release by Graviti Pharmaceuticals Private Limited


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