59923-726 : Erlotinib 100 mg Oral Tablet, Film Coated
NDC: | 59923-726 |
Labeler: | Areva Pharmaceuticals |
Product Type: | Human Prescription Drug |
Drug Name: | Erlotinib |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA211960 |
Rev. Date: |
Appearance:
Markings: | S12 |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 9 |
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:
- 59923-726-30: 1 BOTTLE IN 1 BOX (59923‑726‑30) > 30 TABLET, FILM COATED IN 1 BOTTLE
Active Ingredients:
- Erlotinib Hydrochloride
Dosage Strength:
- 100 mg
Inactive Ingredients:
- Microcrystalline Cellulose
- Lactose Monohydrate
- Sodium Lauryl Sulfate
- Magnesium Stearate
- Hydroxypropyl Cellulose, Unspecified
- Titanium Dioxide
- Polyethylene Glycol, Unspecified
- Sodium Starch Glycolate Type a Potato
- Hypromellose, Unspecified /
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.