75987-010 : Duexis (Famotidine 26.6 mg / Ibuprofen 800 mg) Oral Tablet


NDC75987-010
Labeler: Horizon Pharma Inc.
Product Type: Human Prescription Drug
Drug Name:  Duexis
Dosage Form: Oral Tablet, Coated
Application #: NDA022519
Rev. Date: 


Appearance:


Markings: HZT
Shapes:  Oval
Colors:  Blue
Size (mm): 19
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.

HZT: (75987-010) Duexis (Famotidine 26.6 mg / Ibuprofen 800 mg) Oral Tablet by Horizon Pharma 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:

  • 75987-010-03: 90 TABLET, COATED IN 1 BOTTLE (75987‑010‑03)
  • 75987-010-71: 15 BLISTER PACK IN 1 BLISTER PACK (75987‑010‑71) > 1 TABLET, COATED IN 1 BLISTER PACK
  • 75987-010-72: 9 BLISTER PACK IN 1 CARTON (75987‑010‑72) > 3 TABLET, COATED IN 1 BLISTER PACK

Active Ingredients:

  • Ibuprofen
  • Famotidine

Dosage Strength:

  • 26.6 mg
  • 800 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Lactose
  • Croscarmellose Sodium
  • Silicon Dioxide
  • Magnesium Stearate
  • Water
  • Povidones
  • Titanium Dioxide
  • Polyethylene Glycols
  • Polysorbate 80
  • Polyvinyl Alcohol
  • Hypromelloses
  • Talc
  • Fd&c Blue No. 2
  • Fd&c Blue No. 1

Pharmaceutical Classes:

  • Cyclooxygenase Inhibitors [MoA]
  • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Histamine H2 Receptor Antagonists [MoA]
  • Histamine-2 Receptor Antagonist [EPC]

NDC QR Code

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NDC 75987-010 QR Code

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