69189-0638 : Zafirlukast 20 mg Oral Tablet, Coated


NDC69189-0638
Labeler: Avera Mckennan Hospital
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:

  • 69189-0638-1: 1 TABLET, COATED IN 1 DOSE PACK (69189‑0638‑1)

Active Ingredients:

  • Zafirlukast

Dosage Strength:

  • 20 mg

Inactive Ingredients:

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

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0310-0411 Zafirlukast 10 mg Oral Tablet by Astrazeneca Pharmaceuticals Lp
  • 0310-0412 Zafirlukast 20 mg Oral Tablet by Astrazeneca Pharmaceuticals Lp
  • 0904-6646 Zafirlukast 20 mg Oral Tablet, Coated by Major Pharmaceuticals
  • 49884-303 Zafirlukast 10 mg Oral Tablet by Par Pharmaceutical Inc.
  • 49884-304 Zafirlukast 20 mg Oral Tablet by Par Pharmaceutical Inc.
  • 49884-549 Zafirlukast 10 mg Oral Tablet, Coated by Par Pharmaceutical Inc.
  • 49884-554 Zafirlukast 20 mg Oral Tablet, Coated by Par Pharmaceutical Inc.
  • 50268-805 Zafirlukast 20 mg Oral Tablet, Film Coated by Avpak
  • 55111-625 Zafirlukast 10 mg Oral Tablet by Dr. Reddys Laboratories Limited
  • 55111-626 Zafirlukast 20 mg Oral Tablet by Dr. Reddys Laboratories Limited
  • 68084-059 Zafirlukast 20 mg Oral Tablet by American Health Packaging
  • 68151-1977 Zafirlukast 20 mg Oral Tablet, Film Coated by Carilion Materials Management

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