# METFORMIN HYDROCHLORIDE

NDC: 72789-561
Generic name: METFORMIN 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: 20250825

FDA application: ANDA213320

## Active ingredients

- METFORMIN HYDROCHLORIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-561"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-561
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d087f00-580b-4b9d-80d9-f97930153e72