42292-053 : Erlotinib Hydrochloride Hydrochloride 150 mg Oral Tablet, Film Coated


NDC: 42292-053
Labeler: Mylan Institutional Inc.
Product Type: Human Prescription Drug
Drug Name:  Erlotinib Hydrochloride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA091002
Rev. Date: 


Appearance:


Markings: M;E;33
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:

  • 42292-053-05: 20 BLISTER PACK IN 1 CARTON (42292‑053‑05) > 1 TABLET, FILM COATED IN 1 BLISTER PACK (42292‑053‑01)

Active Ingredients:

  • Erlotinib

Dosage Strength:

  • 150 mg

Inactive Ingredients:

  • Hypromellose 2910 (3 Mpa.s)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Polyethylene Glycol 400
  • Sodium Lauryl Sulfate
  • Sodium Starch Glycolate Type a Potato
  • Titanium Dioxide /

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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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.