FDA NDC Directory · JSON-LD · Markdown
NDC 80513-403 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE
| Generic name | Guaifenesin |
|---|---|
| Labeler / Manufacturer | Advanced Rx LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA213420 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | GUAIFENESIN (600 mg/1) |
| Marketing started | 20200508 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).