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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017355
Company: TEVA BRANDED PHARM
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LOESTRIN FE 1.5/30 ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 0.03MG;1.5MG TABLET;ORAL-21 Discontinued None Yes 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
04/30/1973 ORIG-1 Approval Type 3 - New Dosage Form PRIORITY

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
01/04/2023 SUPPL-57 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/017355s057lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/017355Orig1s057ltr.pdf
04/29/2022 SUPPL-56 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/017355s056lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/017355Orig1s056ltr.pdf
08/09/2017 SUPPL-53 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/017354s051,017355s053,017875s037,017876s036lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/017876Orig1s036,017354Orig1s051,017875s037,017355Orig1s053ltr.pdf
08/05/2014 SUPPL-48 Manufacturing (CMC)

Label is not available on this site.

05/02/2003 SUPPL-46 Labeling Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2003/17354slr044,17355slr046,17875slr032,17876slr031ltr.pdf
03/31/1999 SUPPL-45 Labeling

Label is not available on this site.

11/24/1999 SUPPL-44 Labeling

Label is not available on this site.

01/08/1999 SUPPL-43 Labeling

Label is not available on this site.

01/16/1998 SUPPL-42 Labeling

Label is not available on this site.

11/20/1997 SUPPL-41 Manufacturing (CMC)

Label is not available on this site.

07/28/1997 SUPPL-40 Manufacturing (CMC)

Label is not available on this site.

07/28/1997 SUPPL-39 Manufacturing (CMC)-Control

Label is not available on this site.

07/07/1995 SUPPL-38 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

06/02/1994 SUPPL-37 Manufacturing (CMC)-Packaging

Label is not available on this site.

06/27/1994 SUPPL-36 Manufacturing (CMC)-Control

Label is not available on this site.

03/07/1994 SUPPL-35 Manufacturing (CMC)

Label is not available on this site.

03/08/1996 SUPPL-34 Labeling

Label is not available on this site.

07/09/1993 SUPPL-33 Manufacturing (CMC)-Control

Label is not available on this site.

03/08/1996 SUPPL-32 Labeling

Label is not available on this site.

04/22/1991 SUPPL-31 Manufacturing (CMC)-Packaging

Label is not available on this site.

05/17/1989 SUPPL-30 Manufacturing (CMC)-Packaging

Label is not available on this site.

03/16/1988 SUPPL-29 Manufacturing (CMC)-Packaging

Label is not available on this site.

09/13/1988 SUPPL-28 Labeling

Label is not available on this site.

10/22/1986 SUPPL-27 Labeling

Label is not available on this site.

10/22/1986 SUPPL-26 Manufacturing (CMC)-Packaging

Label is not available on this site.

06/04/1986 SUPPL-25 Labeling

Label is not available on this site.

10/22/1984 SUPPL-24 Labeling

Label is not available on this site.

09/17/1985 SUPPL-23 Manufacturing (CMC)-Control

Label is not available on this site.

11/18/1982 SUPPL-22 Manufacturing (CMC)-Control

Label is not available on this site.

11/09/1981 SUPPL-21 Manufacturing (CMC)-Formulation

Label is not available on this site.

04/06/1981 SUPPL-20 Labeling

Label is not available on this site.

02/08/1977 SUPPL-16 Manufacturing (CMC)-Control

Label is not available on this site.

02/08/1977 SUPPL-15 Manufacturing (CMC)-Control

Label is not available on this site.

11/14/1975 SUPPL-12 Labeling

Label is not available on this site.

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
01/04/2023 SUPPL-57 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/017355s057lbl.pdf
04/29/2022 SUPPL-56 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/017355s056lbl.pdf
08/09/2017 SUPPL-53 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/017354s051,017355s053,017875s037,017876s036lbl.pdf
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