59923-726 : Erlotinib 100 mg Oral Tablet, Film Coated


NDC59923-726
Labeler: Areva Pharmaceuticals
Product Type: Human Prescription Drug
Drug Name:  Erlotinib
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA211960
Rev. Date: 


Appearance:


Markings: S12
Shapes:  Round
Colors:  White
Size (mm): 9
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:

  • 59923-726-30: 1 BOTTLE IN 1 BOX (59923‑726‑30) > 30 TABLET, FILM COATED IN 1 BOTTLE

Active Ingredients:

  • Erlotinib Hydrochloride

Dosage Strength:

  • 100 mg

Inactive Ingredients:

  • Microcrystalline Cellulose
  • Lactose Monohydrate
  • Sodium Lauryl Sulfate
  • Magnesium Stearate
  • Hydroxypropyl Cellulose, Unspecified
  • Titanium Dioxide
  • Polyethylene Glycol, Unspecified
  • Sodium Starch Glycolate Type a Potato
  • Hypromellose, Unspecified /

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 59923-725 Erlotinib 25 mg Oral Tablet, Film Coated by Areva Pharmaceuticals
  • 59923-727 Erlotinib 150 mg Oral Tablet, Film Coated by Areva Pharmaceuticals
  • 0093-7662 Erlotinib 25 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 0093-7663 Erlotinib 100 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 0093-7664 Erlotinib 150 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 31722-263 Erlotinib 25 mg Oral Tablet, Film Coated by Camber Pharmaceuticals, Inc.
  • 31722-264 Erlotinib 100 mg Oral Tablet, Film Coated by Camber Pharmaceuticals, Inc.
  • 31722-265 Erlotinib 150 mg Oral Tablet, Film Coated by Camber Pharmaceuticals, Inc.
  • 51991-890 Erlotinib 25 mg Oral Tablet, Film Coated by Breckenridge Pharmaceutical, Inc.
  • 51991-891 Erlotinib 100 mg Oral Tablet, Film Coated by Breckenridge Pharmaceutical, Inc.
  • 51991-892 Erlotinib 150 mg Oral Tablet, Film Coated by Breckenridge Pharmaceutical, Inc.
  • 59651-530 Erlotinib 25 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 59651-531 Erlotinib 100 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 59651-532 Erlotinib 150 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 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.
  • More related products ...

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 59923-726 QR Code

< Prev: 59923-725Next: 59923-727 >




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.