0069-0502 : Xeljanz 22 mg Oral Tablet, Film Coated, Extended Release
NDC: | 0069-0502 |
Labeler: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | Human Prescription Drug |
Drug Name: | Xeljanz XR |
Dosage Form: | Oral Tablet, Film Coated, Extended Release |
Application #: | NDA208246 |
Rev. Date: |
Appearance:
Markings: | JKI22 |
Shapes: |
Oval |
Colors: |
Brown |
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:
- 0069-0502-30: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0069‑0502‑30)
Active Ingredients:
- Tofacitinib Citrate
Dosage Strength:
- 22 mg
Inactive Ingredients:
- Sorbitol
- Hydroxyethyl Cellulose (140 Mpa.s At 5%)
- Copovidone K25-31
- Magnesium Stearate
- Cellulose Acetate
- Hydroxypropyl Cellulose (1600000 Wamw)
- Titanium Dioxide
- Hypromellose 2910 (6 Mpa.s)
- Triacetin
- Ferric Oxide Red
- Shellac
- Ammonia
- Propylene Glycol
- Ferrosoferric Oxide
- Fd&c Blue No. 2--aluminum Lake
- Ferric Oxide Yellow /
Pharmaceutical Classes:
- Janus Kinase Inhibitor [EPC]
- Janus Kinase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 0069-0501 Xeljanz 11 mg Oral Tablet, Film Coated, Extended Release by Pfizer Laboratories Div Pfizer Inc
- 63539-501 Xeljanz 11 mg Oral Tablet, Extended Release by U.S. Pharmaceuticals
- 63539-502 Xeljanz 22 mg Oral Tablet, Extended Release by U.S. Pharmaceuticals
NDC QR Code
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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.