FDA NDC Directory · JSON-LD · Markdown
NDC 51660-423 · HUMAN OTC DRUG · TABLET, SUGAR COATED
| Generic name | ibuprofen and pseudoephedrine hydrochloride |
|---|---|
| Labeler / Manufacturer | Ohm Laboratories Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA074567 |
| Dosage form / route | TABLET, SUGAR COATED · ORAL |
| Active ingredients | IBUPROFEN (200 mg/1) PSEUDOEPHEDRINE HYDROCHLORIDE (30 mg/1) |
| Marketing started | 20011013 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).