Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 086766
Company: WENDT
Company: WENDT
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
NITROFURAZONE | NITROFURAZONE | 0.2% | OINTMENT;TOPICAL | 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 |
---|---|---|---|---|---|---|---|
05/11/1981 | ORIG-1 | Approval |
Review
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/nda/pre96/086766_S000_NitrofurazoneTOC.cfm |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
02/17/1982 | SUPPL-3 | Manufacturing (CMC) |
Label is not available on this site. |
||
02/17/1982 | SUPPL-1 | Manufacturing (CMC) |
Label is not available on this site. |