# MOXIFLOXACIN HYDROCHLORIDE

NDC: 72789-037
Generic name: moxifloxacin hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140304

FDA application: ANDA202632

## Active ingredients

- MOXIFLOXACIN HYDROCHLORIDE: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a98b20d-c4a1-4184-8387-a4866d1d62bf