FDA NDC Directory · JSON-LD · Markdown
NDC 11523-7162 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE
| Generic name | Loratadine and pseudoephedrine sulfate |
|---|---|
| Labeler / Manufacturer | Bayer HealthCare LLC. |
| Marketing category | New Drug Application (innovator) · App NDA019670 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | LORATADINE (5 mg/1) PSEUDOEPHEDRINE SULFATE (120 mg/1) |
| Marketing started | 20091201 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).