# Metformin Hydrochloride

NDC: 70247-019
Generic name: Metformin Hydrochloride Extended-Release Tablets
Labeler / Manufacturer: Qingdao BAHEAL Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190301

FDA application: ANDA209993

## 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:"70247-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70247-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ea6e623-4073-4671-e053-2a91aa0a3ca3