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Bimatoprost

ANDA 210263, held by Alembic. Bimatoprost.

  • First approved: Apr 12, 2019
  • Review: Standard
  • Supplements approved: 2
  • Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 3 submissions below
DateSubmissionStatusDocuments
Apr 12, 2019Original applicationApprovedNone posted

Products

1 strengths and forms
ProductActive ingredientMarketing
Bimatoprost0.03% · solution/drops;ophthalmicBimatoprostRx
All 3 submissions, including labeling and manufacturing supplements
DateSubmissionStatusDocuments
Dec 20, 2022Supplement 2Labeling · Standard reviewApprovedNone posted
Dec 20, 2022Supplement 3Labeling · Standard reviewApprovedNone posted
Apr 12, 2019Original applicationApprovedNone posted

Identifiers

Application
ANDA 210263

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.