Glumetza
metformin hydrochloride · Tablet, Film Coated, Extended Release · Oral
No FDA structured label text is available for Glumetza. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Metformin Hydrochloride in 3 products
Glumetza NDC products (3)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 68012-002 | Metformin Hydrochloride 500 mg/1 Tablet, Film Coated, Extended Release | Santarus, Inc. | NDA |
| 68012-003 | Metformin Hydrochloride 1000 mg/1 Tablet, Film Coated, Extended Release | Santarus, Inc. | NDA |
| 68012-004 | Metformin Hydrochloride 500 mg/1 Tablet, Film Coated, Extended Release | Santarus, Inc. | NDA |
Frequently asked questions
Who makes Glumetza?
Glumetza is listed by 1 labeler in the FDA NDC directory, including Santarus, Inc..