FDA NDC Directory · JSON-LD · Markdown
NDC 85237-1650 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE
| Generic name | Guaifenesin and Dextromethorphan Hydrobromide |
|---|---|
| Labeler / Manufacturer | Select Consumer Group |
| Marketing category | New Drug Application (innovator) · App NDA021620 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | DEXTROMETHORPHAN HYDROBROMIDE (30 mg/1) GUAIFENESIN (600 mg/1) |
| Marketing started | 20120626 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).