51991-892 : Erlotinib 150 mg Oral Tablet, Film Coated


NDC51991-892
Labeler: Breckenridge Pharmaceutical, Inc.
Product Type: Human Prescription Drug
Drug Name:  Erlotinib
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA208488
Rev. Date: 


Appearance:


Markings: N;150
Shapes:  Round
Colors:  White
Size (mm): 10
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:

  • 51991-892-33: 30 TABLET, FILM COATED IN 1 BOTTLE (51991‑892‑33)

Active Ingredients:

  • Erlotinib Hydrochloride

Dosage Strength:

  • 150 mg

Inactive Ingredients:

  • Hypromellose, Unspecified
  • Lactose Monohydrate
  • Microcrystalline Cellulose
  • Polyethylene Glycol 4000
  • Sodium Lauryl Sulfate
  • Sodium Starch Glycolate Type a Potato
  • Sodium Stearyl Fumarate
  • Titanium Dioxide /

Pharmaceutical Classes:

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

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