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ACTIVASE از شرکت GENENTECH

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ACTIVASE از شرکت GENENTECH

Biologic License Application (BLA): 103172

Company: GENENTECH

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ACTIVASE ALTEPLASE 100MG/VIAL VIAL; SINGLE-USE Prescription

None

No No
ACTIVASE ALTEPLASE 50MG/VIAL VIAL; SINGLE-USE Prescription

None

No No
CATHFLO ACTIVASE ALTEPLASE 2MG/VIAL VIAL Prescription

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
11/13/1987 ORIG-1 Approval

N/A

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
04/08/2020 SUPPL-5267 Supplement

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/103172Orig1s5267ltr.pdf

02/28/2018 SUPPL-5260 Supplement

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/103172s5260lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/103172Orig1s5260ltr.pdf

02/28/2018 SUPPL-5259 Supplement

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/103172s5259lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/103172Orig1s5259ltr.pdf

06/30/2017 SUPPL-5253 Supplement

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/103172s5253lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/103172Orig1s5253ltr.pdf

02/13/2015 SUPPL-5203 Supplement

Label (PDF)

Letter (PDF)

Review (PDF)

Label for ACTIVASE

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/103172s5203lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2015/103172Orig1s5203ltr.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/bla/2015/103172Orig1s5203.pdf

01/04/2005 SUPPL-5071 Supplement

Label (PDF)

Label for CATHFLO ACTIVASE

https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/103172s5071lbl.pdf

05/15/2002 SUPPL-5009 Supplement

Label (PDF)

Letter

https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/altegen051502LB.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/altegen051502L.htm

09/04/2001 SUPPL-5003 Supplement

Label (PDF)

Letter

https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/altegen090401LB.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2001/altegen090401L.htm

06/18/1996 SUPPL-1055 Supplement

Letter (PDF)

Review

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/1996/altegen061896L.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/nda/96/alteplase_toc.cfm

04/03/1995 SUPPL-1036 Supplement

Label is not available on this site.

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
02/28/2018 SUPPL-5260

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/103172s5260lbl.pdf
02/28/2018 SUPPL-5259

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/103172s5259lbl.pdf
06/30/2017 SUPPL-5253

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/103172s5253lbl.pdf
02/13/2015 SUPPL-5203

Labeling

Label (PDF)

Label for ACTIVASE

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/103172s5203lbl.pdf
01/04/2005 SUPPL-5071

Efficacy

Label (PDF)

Label for CATHFLO ACTIVASE

https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/103172s5071lbl.pdf
05/15/2002 SUPPL-5009

Supplement

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/altegen051502LB.pdf
09/04/2001 SUPPL-5003

Efficacy

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/altegen090401LB.pdf
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