49884-554 : Zafirlukast 20 mg Oral Tablet, Coated


NDC: 49884-554
Labeler: Par Pharmaceutical Inc.
Product Type: Human Prescription Drug
Drug Name:  Zafirlukast
Dosage Form: Oral Tablet, Coated
Application #: NDA020547
Rev. Date: 


Appearance:


Shapes:  Round
Colors:  White
Size (mm): 8
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:

  • 49884-554-02: 60 TABLET, COATED IN 1 BOTTLE (49884‑554‑02)

Active Ingredients:

  • Zafirlukast

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Croscarmellose Sodium
  • Lactose, Unspecified Form
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Povidones
  • Hypromelloses
  • Titanium Dioxide

Pharmaceutical Classes:

  • Cytochrome P450 2C9 Inhibitors [MoA]
  • Leukotriene Receptor Antagonist [EPC]
  • Leukotriene Receptor Antagonists [MoA]

Related Products:

Based on records with the same trade name.
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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.