NDC 69367-305
Miglitol
Miglitol
Miglitol is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Westminster Pharmaceuticals, Llc. The primary component is Miglitol.
| Product ID | 69367-305_b8da2294-374a-e57d-e053-2a95a90ab5ca |
| NDC | 69367-305 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Miglitol |
| Generic Name | Miglitol |
| Dosage Form | Tablet, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-01-15 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA203965 |
| Labeler Name | Westminster Pharmaceuticals, LLC |
| Substance Name | MIGLITOL |
| Active Ingredient Strength | 100 mg/1 |
| Pharm Classes | alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |