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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 212436
Company: PFIZER
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
IBRANCE PALBOCICLIB 75MG TABLET;ORAL Prescription None Yes No
IBRANCE PALBOCICLIB 100MG TABLET;ORAL Prescription None Yes No
IBRANCE PALBOCICLIB 125MG TABLET;ORAL 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
11/01/2019 ORIG-1 Approval Type 3 - New Dosage Form STANDARD Label (PDF)
Letter (PDF)
Review
https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212436lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/212436Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/212436Orig1s000TOC.cfm
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
09/06/2023 SUPPL-6 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/212436s005s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/212436Orig1s005,s006ltr.pdf
09/06/2023 SUPPL-5 Efficacy-Labeling Change With Clinical Data Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/212436s005s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/212436Orig1s005,s006ltr.pdf
12/13/2022 SUPPL-3 Efficacy-New Patient Population Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/212436s003lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/207103Orig1s015;212436Orig1s003ltr.pdf
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
09/06/2023 SUPPL-6 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/212436s005s006lbl.pdf
09/06/2023 SUPPL-5 Efficacy-Labeling Change With Clinical Data Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/212436s005s006lbl.pdf
12/13/2022 SUPPL-3 Efficacy-New Patient Population Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/212436s003lbl.pdf
11/01/2019 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212436lbl.pdf
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