Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 021712
Company: UCB INC
Company: UCB INC
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| FLUXID | FAMOTIDINE | 20MG | TABLET, ORALLY DISINTEGRATING;ORAL | Discontinued | None | No | No |
| FLUXID | FAMOTIDINE | 40MG | TABLET, ORALLY DISINTEGRATING;ORAL | Discontinued | None | No | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 09/24/2004 | ORIG-1 | Approval | Type 3 - New Dosage Form | STANDARD |
Label (PDF)
Letter (PDF) Review |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2004/21712lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2004/21712ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2004/021712s000_TOC.cfm |
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
|---|---|---|---|---|---|
| 09/24/2004 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2004/21712lbl.pdf |