68151-1977 : Zafirlukast 20 mg Oral Tablet, Film Coated


NDC: 68151-1977
Labeler: Carilion Materials Management
Product Type: Human Prescription Drug
Drug Name:  Zafirlukast
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA090372
Rev. Date: 


Appearance:


Markings: R;626
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.

R 626: (55111-626) Zafirlukast 20 mg Oral Tablet, Film Coated by Carilion Materials Management
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:

  • 68151-1977-6: 1 TABLET, FILM COATED IN 1 PACKAGE (68151‑1977‑6)

Active Ingredients:

  • Zafirlukast

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Hydroxypropyl Cellulose (Type H)
  • Hypromellose 2910 (5 Mpa.s)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polyethylene Glycol 400
  • Sodium Starch Glycolate Type a Potato
  • Titanium Dioxide

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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  • 49884-303 Zafirlukast 10 mg Oral Tablet by Par Pharmaceutical Inc.
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NDC QR Code

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NDC 68151-1977 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.