Metformin hydrochloride ER is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Northwind Pharmaceuticals. The primary component is Metformin Hydrochloride.
| Product ID | 51655-562_c7ae5667-dab8-42b6-9224-86f284b16536 |
| NDC | 51655-562 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Metformin hydrochloride ER |
| Generic Name | Metformin Hydrochloride Er |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-06-01 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076869 |
| Labeler Name | Northwind Pharmaceuticals |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Active Ingredient Strength | 750 mg/1 |
| Pharm Classes | Biguanide [EPC],Biguanides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2014-06-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076869 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-06-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| METFORMIN HYDROCHLORIDE | 750 mg/1 |
| SPL SET ID: | 5909a843-51d7-4cc2-a2ad-b848463e85b6 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 75834-500 | Metformin hydrochloride ER | Metformin hydrochloride ER |
| 76385-129 | Metformin hydrochloride ER | Metformin hydrochloride ER |
| 51655-550 | Metformin hydrochloride ER | Metformin hydrochloride ER |
| 72789-106 | Metformin hydrochloride ER | Metformin hydrochloride ER |
| 71610-457 | METFORMIN HYDROCHLORIDE ER | METFORMIN HYDROCHLORIDE ER |
| 51655-562 | Metformin hydrochloride | Metformin hydrochloride ER |