FDA NDC Directory · JSON-LD · Markdown
NDC 11523-0102 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE
| Generic name | Loratadine pseudoephedrine sulfate |
|---|---|
| Labeler / Manufacturer | Bayer HealthCare LLC. |
| Marketing category | Abbreviated NDA (generic) · App ANDA075706 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | LORATADINE (10 mg/1) PSEUDOEPHEDRINE SULFATE (240 mg/1) |
| Marketing started | 20221212 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).