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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017876
Company: TEVA BRANDED PHARM
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LOESTRIN 21 1/20 ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 0.02MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET;ORAL-21 Discontinued None Yes No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
10/01/1976 ORIG-1 Approval Type 3 - New Dosage Form STANDARD

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-40 Labeling-Package Insert Label (PDF)
Letter (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/017876s040lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/017876Orig1s040ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/017876Orig1s040ltr.pdf
04/29/2022 SUPPL-39 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/017876s039lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/017876Orig1s039ltr.pdf
08/09/2017 SUPPL-36 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
09/26/2014 SUPPL-33 Manufacturing (CMC)

Label is not available on this site.

05/02/2003 SUPPL-31 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-30 Labeling

Label is not available on this site.

11/24/1999 SUPPL-29 Labeling

Label is not available on this site.

01/08/1999 SUPPL-28 Labeling

Label is not available on this site.

01/16/1998 SUPPL-27 Labeling

Label is not available on this site.

11/20/1997 SUPPL-26 Manufacturing (CMC)

Label is not available on this site.

07/28/1997 SUPPL-25 Manufacturing (CMC)

Label is not available on this site.

07/28/1997 SUPPL-24 Manufacturing (CMC)-Control

Label is not available on this site.

07/07/1995 SUPPL-23 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

06/02/1994 SUPPL-22 Manufacturing (CMC)-Packaging

Label is not available on this site.

06/27/1994 SUPPL-21 Manufacturing (CMC)-Control

Label is not available on this site.

03/08/1996 SUPPL-20 Labeling

Label is not available on this site.

03/07/1994 SUPPL-19 Manufacturing (CMC)

Label is not available on this site.

07/09/1993 SUPPL-18 Manufacturing (CMC)-Control

Label is not available on this site.

03/08/1996 SUPPL-17 Labeling

Label is not available on this site.

04/22/1991 SUPPL-16 Labeling

Label is not available on this site.

05/17/1989 SUPPL-15 Manufacturing (CMC)-Packaging

Label is not available on this site.

03/16/1988 SUPPL-14 Manufacturing (CMC)-Packaging

Label is not available on this site.

09/13/1988 SUPPL-13 Labeling

Label is not available on this site.

06/04/1986 SUPPL-12 Labeling

Label is not available on this site.

10/22/1984 SUPPL-11 Labeling

Label is not available on this site.

09/17/1985 SUPPL-10 Manufacturing (CMC)-Control

Label is not available on this site.

11/18/1982 SUPPL-9 Manufacturing (CMC)-Control

Label is not available on this site.

11/10/1977 SUPPL-5 Labeling

Label is not available on this site.

06/14/1978 SUPPL-4 Manufacturing (CMC)-Control

Label is not available on this site.

02/09/1977 SUPPL-2 Manufacturing (CMC)-Control

Label is not available on this site.

02/09/1977 SUPPL-1 Manufacturing (CMC)-Control

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-40 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/017876s040lbl.pdf
04/29/2022 SUPPL-39 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/017876s039lbl.pdf
08/09/2017 SUPPL-36 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/017354s051,017355s053,017875s037,017876s036lbl.pdf
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