FDA NDC Directory · JSON-LD · Markdown
NDC 69668-515 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE
| Generic name | DOXYCYCLINE HYCLATE |
|---|---|
| Labeler / Manufacturer | Sonoma Pharmaceuticals, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA207494 |
| Dosage form / route | TABLET, DELAYED RELEASE · ORAL |
| Active ingredients | DOXYCYCLINE HYCLATE (150 mg/1) |
| Marketing started | 20161128 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).