NDC product
Guaifenesin 600 mg
NDC 25000-042 · MARKSANS PHARMA LIMITED
Key facts
| Product NDC | 25000-042 |
|---|---|
| Proprietary name | Guaifenesin 600 mg |
| Nonproprietary name | Guaifenesin 600 mg |
| Substances | GUAIFENESIN |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | MARKSANS PHARMA LIMITED |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA217780 |
| Pharmacologic classes | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE] |
| Marketing start | Aug 23, 2023 |
| 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: