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Rifampin

ANDA 206736, held by Watson Pharms Teva. Rifampin.

  • First approved: Jan 19, 2016
  • Review: Standard
  • 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
Jan 19, 2016Original applicationApprovedNone posted

Products

1 strengths and forms
ProductActive ingredientMarketing
Rifampin600MG/VIAL · injectable;injectionRifampinDiscontinued
All 4 submissions, including labeling and manufacturing supplements
DateSubmissionStatusDocuments
Jul 6, 2020Supplement 3Labeling · Standard reviewApprovedNone posted
Jul 6, 2020Supplement 2Labeling · Standard reviewApprovedNone posted
Jul 6, 2020Supplement 1Labeling · Standard reviewApprovedNone posted
Jan 19, 2016Original applicationApprovedNone posted

Identifiers

Application
ANDA 206736

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.