# METRONIDAZOLE

NDC: 61919-032
Generic name: METRONIDAZOLE
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190821

FDA application: ANDA203458

## Active ingredients

- METRONIDAZOLE: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61919-032"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-032
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=90a5acb3-f8cc-1e82-e053-2995a90a4e97