# Metformin hydrochloride

NDC: 70518-4652
Generic name: Metformin hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260504

FDA application: ANDA213651

## Active ingredients

- METFORMIN HYDROCHLORIDE: 1000 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4652"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4652
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=014f2a32-8440-4d0c-8f5d-c4b3a49e0dec