FDA NDC Directory · JSON-LD · Markdown
NDC 73581-201 · HUMAN OTC DRUG · TABLET
| Generic name | LEVOCETIRIZINE DIHYDROCHLORIDE |
|---|---|
| Labeler / Manufacturer | YYBA CORP |
| Marketing category | Abbreviated NDA (generic) · App ANDA213513 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | LEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1) |
| Marketing started | 20200630 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).