NDC 68682-021-50
Metformin hydrochloride 500 mg/1
metformin hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
Metformin hydrochloride is a tablet, film coated, extended release containing metformin hydrochloride at a strength of 500 mg/1. Manufactured by Oceanside Pharmaceuticals.
Key Facts
- Brand Name
- Metformin hydrochloride
- Generic Name
- metformin hydrochloride
- NDC Code (Package)
68682-021-50- NDC Code (Product)
68682-021- Manufacturer
- Oceanside Pharmaceuticals
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA021748
- Marketing Start
- 03/20/2018
Recall History
No Recall HistoryView Full Drug Page
Metformin hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.