FDA NDC Directory · JSON-LD · Markdown
NDC 73581-401 · HUMAN OTC DRUG · TABLET
| Generic name | GUAIFENESIN |
|---|---|
| Labeler / Manufacturer | YYBA CORP |
| Marketing category | Abbreviated NDA (generic) · App ANDA213420 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | GUAIFENESIN (600 mg/1) |
| Marketing started | 20220302 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).