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CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER از شرکت B BRAUN

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CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER از شرکت B BRAUN

New Drug Application (NDA): 050821

Company: B BRAUN

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER CEFEPIME HYDROCHLORIDE EQ 1GM BASE/VIAL INJECTABLE;INJECTION Prescription

None

No No
CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER CEFEPIME HYDROCHLORIDE EQ 2GM BASE/VIAL INJECTABLE;INJECTION 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
05/06/2010 ORIG-1 Approval

Type 5 – New Formulation or New Manufacturer

STANDARD

Label (PDF)

Letter (PDF)

Review

Summary Review (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/050821s000lbl.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2010/050821s000ltr.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/050821_cefepime_toc.cfm
https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/050821s000SumR.pdf

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
11/09/2015 SUPPL-4 Labeling-Package Insert

Label (PDF)

Letter (PDF)

Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs.

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/050821s004lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2015/050821Orig1s004ltr.pdf

06/06/2014 SUPPL-2 Labeling-Package Insert, Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/050821s002lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/050821Orig1s002ltr.pdf

09/06/2012 SUPPL-1 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050821s001lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/050821Orig1s001ltr.pdf

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
11/09/2015 SUPPL-4

Labeling-Package Insert

Label (PDF)

Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs.

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/050821s004lbl.pdf
06/06/2014 SUPPL-2

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/050821s002lbl.pdf
06/06/2014 SUPPL-2

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/050821s002lbl.pdf
09/06/2012 SUPPL-1

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/050821s001lbl.pdf
05/06/2010 ORIG-1 Approval

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/050821s000lbl.pdf
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