FDA NDC Directory · JSON-LD · Markdown
NDC 67751-146 · HUMAN OTC DRUG · TABLET, COATED
| Generic name | IBUPROFEN |
|---|---|
| Labeler / Manufacturer | Navajo Manufacturing Company Inc. |
| Marketing category | New Drug Application (innovator) · App NDA018989 |
| Dosage form / route | TABLET, COATED · ORAL |
| Active ingredients | IBUPROFEN (200 mg/1) |
| Marketing started | 20160920 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).