FDA NDC Directory · JSON-LD · Markdown
NDC 37808-935 · HUMAN OTC DRUG · TABLET
| Generic name | Guaifenesin |
|---|---|
| Labeler / Manufacturer | H E B |
| Marketing category | Abbreviated NDA (generic) · App ANDA207342 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | GUAIFENESIN (600 mg/1) |
| Marketing started | 20210528 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).