FDA NDC Directory · JSON-LD · Markdown
NDC 51655-680 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | Citalopram Hydrobromide |
|---|---|
| Labeler / Manufacturer | Northwind Health Company, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA077031 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | CITALOPRAM HYDROBROMIDE (20 mg/1) |
| Marketing started | 20220302 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).