FDA NDC Directory · JSON-LD · Markdown
NDC 67751-192 · HUMAN OTC DRUG · TABLET, FILM COATED
| Generic name | Cetirizine Hydrochloride |
|---|---|
| Labeler / Manufacturer | Navajo Manufacturing Company Incorporated |
| Marketing category | New Drug Application (innovator) · App NDA019835 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | CETIRIZINE HYDROCHLORIDE (10 mg/1) |
| Marketing started | 20191120 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).