0093-7663 : Erlotinib 100 mg Oral Tablet, Film Coated


NDC: 0093-7663
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Erlotinib
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA091059
Rev. Date: 


Appearance:


Markings: TEVA;7663
Shapes:  Round
Colors:  White
Size (mm): 8
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:

  • 0093-7663-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0093‑7663‑56)

Active Ingredients:

  • Erlotinib Hydrochloride

Dosage Strength:

  • 100 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Hypromellose 2910 (3 Mpa.s)
  • Hypromellose 2910 (6 Mpa.s)
  • Hypromellose 2910 (50 Mpa.s)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polydextrose
  • Polyethylene Glycol 8000
  • Sodium Lauryl Sulfate
  • Sodium Starch Glycolate Type a Potato
  • Titanium Dioxide
  • Triacetin /

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.