NDC product
GRANULE · Unilab Pharmaceuticals and Chemicals Private Limited
NDC 25119-8000 · Unilab Pharmaceuticals and Chemicals Private Limited
Key facts
| Product NDC | 25119-8000 |
|---|---|
| Nonproprietary name | Guaifenesin 95% DC |
| Substances | GUAIFENESIN |
| Dosage form | GRANULE |
| Labeler | Unilab Pharmaceuticals and Chemicals Private Limited |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Oct 1, 2025 |
| 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: