71332-001 : Tavalisse 100 mg Oral Tablet
NDC: | 71332-001 |
Labeler: | Rigel Pharmaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Tavalisse |
Dosage Form: | Oral Tablet |
Application #: | NDA209299 |
Rev. Date: |
Appearance:
Markings: | 100;R |
Shapes: |
Round |
Colors: |
Orange |
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:
- 71332-001-01: 60 TABLET IN 1 BOTTLE (71332‑001‑01)
Active Ingredients:
- Fostamatinib
Dosage Strength:
- 100 mg
Inactive Ingredients:
- Mannitol
- Sodium Bicarbonate
- Sodium Starch Glycolate Type a Potato
- Povidone, Unspecified
- Magnesium Stearate
- Polyvinyl Alcohol, Unspecified
- Titanium Dioxide
- Polyethylene Glycol 3350
- Talc
- Ferric Oxide Yellow
- Ferric Oxide Red /
Related Products:
Based on records with the same trade name.- 71332-002 Tavalisse 150 mg Oral Tablet by Rigel Pharmaceuticals, Inc.
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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.