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BECONASE AQ از شرکت GLAXOSMITHKLINE

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داروی نمایش داده شده مورد تایید FDA می باشد و اطلاعات ثبت آن در زیر قابل مشاهده است

BECONASE AQ از شرکت GLAXOSMITHKLINE

New Drug Application (NDA): 019389

Company: GLAXOSMITHKLINE

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BECONASE AQ BECLOMETHASONE DIPROPIONATE MONOHYDRATE EQ 0.042MG DIPROP/SPRAY SPRAY, METERED;NASAL Prescription

None

Yes Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
07/27/1987 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
04/12/2019 SUPPL-34 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019389Orig1s034lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/019389Orig1s034ltr.pdf

06/17/2014 SUPPL-33 Manufacturing (CMC)

Label is not available on this site.

10/27/2005 SUPPL-27 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/019389s027lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/019389s027ltr.pdf

03/04/2002 SUPPL-26 Manufacturing (CMC)-Control

Label is not available on this site.

12/16/2002 SUPPL-25 Labeling

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/19389slr025ltr.pdf

07/09/2001 SUPPL-24 Manufacturing (CMC)-Control

Label is not available on this site.

08/31/2001 SUPPL-23 Labeling

Label (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/19389s23lbl.pdf

12/19/2002 SUPPL-21 Labeling

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/19389slr021ltr.pdf

02/24/1999 SUPPL-20 Manufacturing (CMC)

Label is not available on this site.

03/27/1998 SUPPL-19 Manufacturing (CMC)

Label is not available on this site.

05/30/1997 SUPPL-17 Labeling

Label is not available on this site.

11/26/1996 SUPPL-16 Labeling

Label is not available on this site.

11/19/1993 SUPPL-12 Labeling

Label is not available on this site.

08/10/1992 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

10/06/1992 SUPPL-9 Manufacturing (CMC)-Control

Label is not available on this site.

05/15/1990 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

09/07/1989 SUPPL-6 Manufacturing (CMC)-Packaging

Label is not available on this site.

03/09/1989 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

12/19/1988 SUPPL-4 Labeling

Label is not available on this site.

07/08/1988 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

08/25/1989 SUPPL-2 Manufacturing (CMC)-Control

Label is not available on this site.

08/19/1988 SUPPL-1 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
04/12/2019 SUPPL-34

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019389Orig1s034lbl.pdf
10/27/2005 SUPPL-27

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/019389s027lbl.pdf
08/31/2001 SUPPL-23

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/19389s23lbl.pdf
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