NDC 0115-2142
COLESTIPOL HYDROCHLORIDE
Colestipol Hydrochloride
COLESTIPOL HYDROCHLORIDE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Amneal Pharmaceuticals Of New York Llc. The primary component is Colestipol Hydrochloride.
| Product ID | 0115-2142_64268362-73d9-44bd-b56a-00164facfe60 |
| NDC | 0115-2142 |
| Product Type | Human Prescription Drug |
| Proprietary Name | COLESTIPOL HYDROCHLORIDE |
| Generic Name | Colestipol Hydrochloride |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-08-17 |
| Marketing Category | ANDA / |
| Application Number | ANDA077510 |
| Labeler Name | Amneal Pharmaceuticals of New York LLC |
| Substance Name | COLESTIPOL HYDROCHLORIDE |
| Active Ingredient Strength | 1 g/1 |
| Pharm Classes | Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |