31722-008 : Zafirlukast 20 mg Oral Tablet, Film Coated


NDC: 31722-008
Labeler: Camber Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Zafirlukast
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA212475
Rev. Date: 


Appearance:


Markings: V;17
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:

  • 31722-008-01: 10 BLISTER PACK IN 1 CARTON (31722‑008‑01) > 10 TABLET, FILM COATED IN 1 BLISTER PACK
  • 31722-008-05: 500 TABLET, FILM COATED IN 1 BOTTLE (31722‑008‑05)
  • 31722-008-60: 60 TABLET, FILM COATED IN 1 BOTTLE (31722‑008‑60)

Active Ingredients:

  • Zafirlukast

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Croscarmellose Sodium
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Povidone K30
  • Titanium Dioxide
  • Hypromellose 2910 (6 Mpa.s) /

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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  • 0310-0411 Zafirlukast 10 mg Oral Tablet by Astrazeneca Pharmaceuticals Lp
  • 0310-0412 Zafirlukast 20 mg Oral Tablet by Astrazeneca Pharmaceuticals Lp
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  • 16571-654 Zafirlukast 10 mg Oral Tablet by Rising Pharmaceuticals, Inc.
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  • 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.
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  • 55111-626 Zafirlukast 20 mg Oral Tablet by Dr. Reddys Laboratories Limited
  • 59651-291 Zafirlukast 10 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
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  • 63629-2102 Zafirlukast 10 mg Oral Tablet, Coated by Bryant Ranch Prepack
  • 64380-187 Zafirlukast 10 mg Oral Tablet, Coated by Strides Pharma Science Limited
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NDC QR Code

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NDC 31722-008 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.