FDA NDC Directory · JSON-LD · Markdown
NDC 41250-728 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | cetirizine hydrochloride, pseudoephedrine hydrochloride |
|---|---|
| Labeler / Manufacturer | Meijer Distribution Inc |
| Marketing category | Abbreviated NDA (generic) · App ANDA210719 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | CETIRIZINE HYDROCHLORIDE (5 mg/1) PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1) |
| Marketing started | 20200407 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).