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NDC 0069-0502 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | tofacitinib |
|---|---|
| Labeler / Manufacturer | Pfizer Laboratories Div Pfizer Inc |
| Marketing category | New Drug Application (innovator) · App NDA208246 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | TOFACITINIB CITRATE (22 mg/1) |
| Marketing started | 20200121 |
| Package count | 1 |
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