FDA NDC Directory · JSON-LD · Markdown
NDC 0113-2219 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE
| Generic name | dextromethorphan hydrobromide, guaifenesin |
|---|---|
| Labeler / Manufacturer | L. Perrigo Company |
| Marketing category | Abbreviated NDA (generic) · App ANDA207602 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | DEXTROMETHORPHAN HYDROBROMIDE (30 mg/1) GUAIFENESIN (600 mg/1) |
| Marketing started | 20190710 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).