NDC 50228-503-30
Metformin Hydrochloride 500 mg/1
Metformin Hydrochloride Extended-Release Tablets · TABLET, FILM COATED, EXTENDED RELEASE
Metformin Hydrochloride is a tablet, film coated, extended release containing metformin hydrochloride extended-release tablets at a strength of 500 mg/1. Manufactured by ScieGen Pharmaceuticals, Inc..
Package Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-503-30)
Key Facts
- Brand Name
- Metformin Hydrochloride
- Generic Name
- Metformin Hydrochloride Extended-Release Tablets
- NDC Code (Package)
50228-503-30- NDC Code (Product)
50228-503- Manufacturer
- ScieGen Pharmaceuticals, Inc.
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA214629
- Marketing Start
- 02/22/2022
Recall History
No Recall HistoryView Full Drug Page
Metformin Hydrochloride — All PackagesOther Packages of NDC 50228-503
- 50228-503-05
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-503-05)
- 50228-503-60
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-503-60)
Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.