glipizide and metformin hcl is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Glipizide; Metformin Hydrochloride.
| Product ID | 50090-1082_f1fe0855-c9c3-4edd-898a-1a3dcdbfe6b4 |
| NDC | 50090-1082 |
| Product Type | Human Prescription Drug |
| Proprietary Name | glipizide and metformin hcl |
| Generic Name | Glipizide And Metformin Hcl |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-06-29 |
| Marketing Category | ANDA / |
| Application Number | ANDA078728 |
| Labeler Name | A-S Medication Solutions |
| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
| Active Ingredient Strength | 5 mg/1; mg/1 |
| Pharm Classes | Biguanide [EPC],Biguanides [CS],Sulfonylurea [EPC],Sulfonylurea Compounds [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2014-11-28 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA078728 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2018-10-01 |
| Marketing End Date | 2018-10-01 |
| Marketing Category | ANDA |
| Application Number | ANDA078728 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-11-28 |
| Marketing End Date | 2017-04-30 |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 23155-115 | glipizide and metformin hcl | glipizide and metformin hcl |
| 23155-116 | glipizide and metformin hcl | glipizide and metformin hcl |
| 23155-117 | glipizide and metformin hcl | glipizide and metformin hcl |
| 50090-1082 | glipizide and metformin hcl | glipizide and metformin hcl |
| 70518-1594 | Glipizide and Metformin HCl | Glipizide and Metformin HCl |
| 70518-2196 | Glipizide and Metformin HCl | Glipizide and Metformin HCl |
| 71205-270 | Glipizide and Metformin HCl | Glipizide and Metformin HCl |