Glipizide and Metformin HCl is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Glipizide; Metformin Hydrochloride.
| Product ID | 70518-2196_8d502408-5250-4e6c-e053-2995a90a2198 |
| NDC | 70518-2196 |
| 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 | 2019-07-09 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA078728 |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
| Active Ingredient Strength | 3 mg/1; mg/1 |
| Pharm Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-07-09 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA078728 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-07-09 |
| Ingredient | Strength |
|---|---|
| GLIPIZIDE | 2.5 mg/1 |
| SPL SET ID: | 328b702b-d901-4d74-b395-6ebb9e65f125 |
| Manufacturer | |
| UNII |
| 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 |