0093-7662 : Erlotinib 25 mg Oral Tablet, Film Coated


NDC0093-7662
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Erlotinib
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA091059
Rev. Date: 


NDC Package Codes:

  • 0093-7662-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0093‑7662‑56)

Active Ingredients:

  • Erlotinib Hydrochloride

Dosage Strength:

  • 25 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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  • 63304-095 Erlotinib 25 mg Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 63304-096 Erlotinib 100 mg Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 63304-135 Erlotinib 150 mg Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 68382-913 Erlotinib 25 mg Oral Tablet by Zydus Pharmaceuticals (Usa) Inc.
  • 68382-914 Erlotinib 100 mg Oral Tablet by Zydus Pharmaceuticals (Usa) Inc.
  • 68382-915 Erlotinib 150 mg Oral Tablet by Zydus Pharmaceuticals (Usa) Inc.
  • 70771-1521 Erlotinib 25 mg Oral Tablet, Film Coated by Cadila Healthcare Limited
  • 70771-1522 Erlotinib 100 mg Oral Tablet, Film Coated by Cadila Healthcare Limited
  • 70771-1523 Erlotinib 150 mg Oral Tablet, Film Coated by Cadila Healthcare Limited
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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.