59651-532 : Erlotinib 150 mg Oral Tablet, Film Coated


NDC: 59651-532
Labeler: Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Drug Name:  Erlotinib
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA216342
Rev. Date: 


NDC Package Codes:

  • 59651-532-03: 30 TABLET, FILM COATED IN 1 BOTTLE (59651‑532‑03)
  • 59651-532-10: 1 BLISTER PACK IN 1 CARTON (59651‑532‑10) > 10 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Erlotinib Hydrochloride

Dosage Strength:

  • 150 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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  • 68382-913 Erlotinib 25 mg Oral Tablet by Zydus Pharmaceuticals (Usa) Inc.
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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.