# Metformin Hydrochloride

NDC: 50228-504
Generic name: Metformin Hydrochloride Extended-Release Tablets
Labeler / Manufacturer: ScieGen Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220222

FDA application: ANDA214629

## 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:"50228-504"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50228-504
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=16dc4008-7b5e-4c6d-9bc8-8db96be911a1