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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 208390
Company: WATSON LABS INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
TICAGRELOR TICAGRELOR 60MG TABLET;ORAL Discontinued None No No
TICAGRELOR TICAGRELOR 90MG TABLET;ORAL Discontinued 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
09/04/2018 ORIG-1 Approval STANDARD Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/208390Orig1s000TAltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
03/14/2024 SUPPL-2 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

03/14/2024 SUPPL-1 Labeling-Package Insert, Labeling-Medication Guide, Labeling-Patient Package Insert

Label is not available on this site.

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