0480-4053 : Gefitinib 250 mg Oral Tablet, Film Coated


NDC: 0480-4053
Labeler: Teva Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Gefitinib
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA208913
Rev. Date: 


NDC Package Codes:

  • 0480-4053-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0480‑4053‑56)

Active Ingredients:

  • Gefitinib

Dosage Strength:

  • 250 mg

Pharmaceutical Classes:

  • Kinase Inhibitor [EPC]
  • Protein Kinase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 50742-366 Gefitinib 250 mg Oral Tablet, Coated by Ingenus Pharmaceuticals, LLC
  • 60505-4512 Gefitinib 250 mg Oral Tablet by Apotex Corp.
  • 67184-0531 Gefitinib 250 mg Oral Tablet, Coated by Qilu Pharmaceutical Co., Ltd.
  • 69339-168 Gefitinib 250 mg Oral Tablet, Film Coated by Dash Pharmaceuticals LLC

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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.