NDC product
Colestipol hydrochloride
NDC 70710-1467 · Zydus Pharmaceuticals USA Inc.
Key facts
| Product NDC | 70710-1467 |
|---|---|
| Proprietary name | Colestipol hydrochloride |
| Nonproprietary name | Colestipol hydrochloride |
| Substances | COLESTIPOL HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Zydus Pharmaceuticals USA Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA215223 |
| Pharmacologic classes | Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA] |
| Marketing start | May 4, 2022 |
| 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: