Drugs@FDA: FDA Approved Drug Products

Home | Previous Page

Abbreviated New Drug Application (ANDA): 074873
Company: TEVA PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
TRETINOIN TRETINOIN 0.05% SOLUTION;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
06/19/1998 ORIG-1 Approval Letter (PDF)
Review (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/1998/74873ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/anda/98/74873ap.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
10/31/2001 SUPPL-6 Manufacturing (CMC)-Facility

Label is not available on this site.

10/31/2001 SUPPL-5 Manufacturing (CMC)-Facility

Label is not available on this site.

10/31/2001 SUPPL-4 Manufacturing (CMC)-Facility

Label is not available on this site.

01/23/2002 SUPPL-3 Manufacturing (CMC)-Facility

Label is not available on this site.

02/26/2001 SUPPL-2 Manufacturing (CMC)-Facility

Label is not available on this site.

03/23/1999 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English