FDA NDC Directory · JSON-LD · Markdown
NDC 68016-531 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
|---|---|
| Labeler / Manufacturer | CHAIN DRUG CONSORTIUM,LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA090922 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | CETIRIZINE HYDROCHLORIDE (5 mg/1) PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1) |
| Marketing started | 20160817 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).