NDC product
Colesevelam Hydrochloride
NDC 0115-1320 · Amneal Pharmaceuticals of New York LLC
Key facts
| Product NDC | 0115-1320 |
|---|---|
| Proprietary name | Colesevelam Hydrochloride |
| Nonproprietary name | COLESEVELAM HYDROCHLORIDE |
| Substances | COLESEVELAM HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Amneal Pharmaceuticals of New York LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA091600 |
| Pharmacologic classes | Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA] |
| Marketing start | May 17, 2018 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: