NDC product
Pyrantel Pamoate
NDC 58988-1760 · ProMex LLC
Key facts
| Product NDC | 58988-1760 |
|---|---|
| Proprietary name | Pyrantel Pamoate |
| Nonproprietary name | Pyrantel Pamoate |
| Substances | PYRANTEL PAMOATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | ProMex LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part357B |
| Marketing start | Sep 27, 2002 |
| Listing certified through | Dec 31, 2026 |
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: