NDC 70700-835 - Joyeaux
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70700-835
- Manufacturer
- Xiromed, LLC | Xiromed Pharma Espana, S.L. | Laboratorios León Farma, S.A.
- Effective date
- 2024-10-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Joyeaux | Xiromed, LLC | Xiromed Pharma Espana, S.L. | Laboratorios León Farma, S.A. | 2024-10-18 | HUMAN PRESCRIPTION DRUG LABEL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Femynor | NORGESTIMATE AND ETHINYL ESTRADIOL | Amneal Pharmaceuticals NY LLC | 59bce25b-ee2c-4f06-afff-e5141d063602 | 2016-05-30 | Boxed warning, Warnings, Adverse reactions | 748797 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.