FDA NDC Directory · JSON-LD · Markdown
NDC 83112-101 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Health Department, Oklahoma State |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA062269 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | DOXYCYCLINE HYCLATE (100 mg/1) |
| Marketing started | 20161001 |
| Marketing ended | 20260630 |
| Package count | 0 |
Source: openFDA. Public-domain (CC0).