FDA NDC Directory · JSON-LD · Markdown
NDC 0363-1604 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE
| Generic name | Guaifenesin and Pseudoephedrine HCL |
|---|---|
| Labeler / Manufacturer | Walgreens Company |
| Marketing category | Abbreviated NDA (generic) · App ANDA208369 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | GUAIFENESIN (600 mg/1) PSEUDOEPHEDRINE HYDROCHLORIDE (60 mg/1) |
| Marketing started | 20190813 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).