Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 002918
Company: POYTHRESS

Products on NDA 002918

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
BENSULFOID	SULFUR	33.32%	POWDER;TOPICAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for NDA 002918

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
09/17/1940	ORIG-1	Approval		UNKNOWN	Review (PDF)	Label is not available on this site.	https://www.accessdata.fda.gov/drugsatfda_docs/nda/pre96/002918Orig1s000.pdf