NDC 61314-231-25 - Diclofenac Sodium
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
- 61314-231
- Requested NDC
- 61314-231-25
- Package NDCs from labels
- 61314-231-25, 61314-231-26, 61314-231-05
- Manufacturer
- FALCON Pharmaceuticals, Ltd.
- Effective date
- 2006-07-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diclofenac Sodium Ophthalmic Solution, 0.1% | FALCON Pharmaceuticals, Ltd. | 2006-07-03 | Human Prescription Drug Label |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| 40B89FD8-6514-7627-58CA-2A258B6B34A2 | 11bf60e0-d81d-4bd3-ac1b-376151d2754d | 2006-07-03 | Warnings, Adverse reactions | 40B89FD8-6514-7627-58CA-2A258B6B34A2 11bf60e0-d81d-4bd3-ac1b-376151d2754d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.