FDA NDC Directory · JSON-LD · Markdown
NDC 59212-562 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | Hydroxychloroquine Sulfate |
|---|---|
| Labeler / Manufacturer | Advanz Pharma (US) Corp. |
| Marketing category | New Drug Application (innovator) · App NDA009768 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | HYDROXYCHLOROQUINE SULFATE (200 mg/1) |
| Marketing started | 20130628 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).