NDC 0009-0199 - Florone
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
- 0009-0199
- Package NDCs from labels
- 0009-0199-31, 0009-0199-60
- Manufacturer
- Pharmacia and Upjohn Division of Pfizer
- Effective date
- 2006-02-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Florone - Pharmacia and Upjohn Division of Pfizer | Pharmacia and Upjohn Division of Pfizer | 2006-02-06 | HUMAN PRESCRIPTION DRUG LABELING |
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 |
|---|---|---|---|---|---|---|
| DF816824-1E51-35C2-75C5-F478BDA631E8 | A0067DCB-4FEA-4A88-A0B1-315A2C21966C | 2006-02-06 | Adverse reactions | DF816824-1E51-35C2-75C5-F478BDA631E8 A0067DCB-4FEA-4A88-A0B1-315A2C21966C |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.