68382-915 : Erlotinib 150 mg Oral Tablet


NDC: 68382-915
Labeler: Zydus Pharmaceuticals (Usa) Inc.
Product Type: Human Prescription Drug
Drug Name:  Erlotinib
Dosage Form: Oral Tablet
Application #: ANDA213065
Rev. Date: 


Appearance:


Markings: 915
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:

  • 68382-915-06: 30 TABLET IN 1 BOTTLE (68382‑915‑06)
  • 68382-915-16: 90 TABLET IN 1 BOTTLE (68382‑915‑16)
  • 68382-915-84: 3 BLISTER PACK IN 1 CARTON (68382‑915‑84) > 10 TABLET IN 1 BLISTER PACK (68382‑915‑30)

Active Ingredients:

  • Erlotinib Hydrochloride

Dosage Strength:

  • 150 mg

Inactive Ingredients:

  • Crospovidone (15 Mpa.s At 5%)
  • Hypromellose 2910 (6 Mpa.s)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose 101
  • Microcrystalline Cellulose 102
  • Polyethylene Glycol 4000
  • Silicon Dioxide
  • Sodium Lauryl Sulfate
  • Talc
  • 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.