NDC 47335-306-83
Metformin Hydrochloride 1000 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 1000 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Metformin Hydrochloride
- Generic Name
- Metformin Hydrochloride
- NDC Code (Package)
47335-306-83- NDC Code (Product)
47335-306- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 1000 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA202917
- Marketing Start
- 05/22/2018
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.