Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 021754
Company: FUJISAWA HLTHCARE
Company: FUJISAWA HLTHCARE
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
MYCAMINE | MICAFUNGIN SODIUM | 50MG | INJECTABLE; INJECTION | Prescription | 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 |
---|---|---|---|---|---|---|---|
03/16/2005 | ORIG-1 | Approval | Type 6 - New Indication (no longer used) | STANDARD |
Label (PDF)
Letter (PDF) Review |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/21506,21754lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/21506,21754ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021754s000_mycamine_TOC.cfm |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
03/16/2005 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/21506,21754lbl.pdf |