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Bimatoprost

ANDA 202719, held by Sandoz. Bimatoprost.

  • First approved: Apr 19, 2016
  • Supplements approved: 3
  • Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 4 submissions below
DateSubmissionStatusDocuments
Apr 19, 2016Original applicationApprovedNone posted

Products

1 strengths and forms
ProductActive ingredientMarketing
Bimatoprost0.03% · solution/drops;topicalBimatoprostRx
All 4 submissions, including labeling and manufacturing supplements
DateSubmissionStatusDocuments
Nov 8, 2022Supplement 5Labeling · Standard reviewApprovedNone posted
Nov 8, 2022Supplement 2Labeling · Standard reviewApprovedNone posted
Aug 12, 2020Supplement 1Labeling · Standard reviewApprovedNone posted
Apr 19, 2016Original applicationApprovedNone posted

Identifiers

Application
ANDA 202719
Company
Sandoz

Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed weekly; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.