FDA NDC Directory · JSON-LD · Markdown
NDC 79481-0709 · HUMAN OTC DRUG · TABLET, MULTILAYER, EXTENDED RELEASE
| Generic name | guaifenesin and pseudoephedrine hydrochloride |
|---|---|
| Labeler / Manufacturer | Meijer, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA214407 |
| Dosage form / route | TABLET, MULTILAYER, EXTENDED RELEASE · ORAL |
| Active ingredients | GUAIFENESIN (600 mg/1) PSEUDOEPHEDRINE HYDROCHLORIDE (60 mg/1) |
| Marketing started | 20250107 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).