Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 215331
Company: MAIA PHARMS INC
Company: MAIA PHARMS INC
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
BORTEZOMIB | BORTEZOMIB | 3.5MG/3.5ML (1MG/ML) | SOLUTION;INTRAVENOUS | Discontinued | None | Yes | No |
BORTEZOMIB | BORTEZOMIB | 3.5MG/1.4ML (2.5MG/ML) | SOLUTION;INTRAVENOUS | Discontinued | None | Yes | 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 |
---|---|---|---|---|---|---|---|
07/27/2022 | ORIG-1 | Approval | Type 5 - New Formulation or New Manufacturer | STANDARD |
Label (PDF)
Letter (PDF) Review |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/215331s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/215331Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2023/215331Orig1s000TOC.cfm |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
07/27/2022 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/215331s000lbl.pdf |