Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 086766
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.

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