59923-727 : Erlotinib 150 mg Oral Tablet, Film Coated


NDC: 59923-727
Labeler: Areva Pharmaceuticals
Product Type: Human Prescription Drug
Drug Name:  Erlotinib
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA211960
Rev. Date: 


Appearance:


Markings: S11
Shapes:  Round
Colors:  White
Size (mm): 11
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:

  • 59923-727-30: 1 BOTTLE IN 1 BOX (59923‑727‑30) > 30 TABLET, FILM COATED IN 1 BOTTLE

Active Ingredients:

  • Erlotinib Hydrochloride

Dosage Strength:

  • 150 mg

Inactive Ingredients:

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

Pharmaceutical Classes:

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

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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.