Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 020013
Company: PHARMACIA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
MAXAQUIN LOMEFLOXACIN HYDROCHLORIDE EQ 400MG BASE TABLET;ORAL Discontinued None No No
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
03/16/2005 SUPPL-15 Labeling Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/20013s015lbl.pdf
03/06/2004 SUPPL-14 Labeling Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2004/20013slr014_mazaquin_lbl.pdf
10/24/2001 SUPPL-8 Labeling Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/20013s8lbl.pdf

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