NDC 0061-5327 - Nuflor Gold
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
- 0061-5327
- Package NDCs from labels
- 0061-5327-01, 0061-5327-02, 0061-5327-03
- Manufacturer
- Schering Corporation | Essex Animal Health Friesoythe
- Effective date
- 2009-09-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Nuflor Gold - Schering Corporation | Essex Animal Health Friesoythe | Schering Corporation | Essex Animal Health Friesoythe | 2009-09-21 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Florfenicol | ACTIVE INGREDIENT | 9J97307Y1H | NUFLOR GOLD (FLORFENICOL) INJECTION [SCHERING CORPORATION] | 1 | |
| Florfenicol | ACTIVE MOIETY | 9J97307Y1H | NUFLOR GOLD (FLORFENICOL) INJECTION [SCHERING CORPORATION] | 1 | |
| Triacetin | INACTIVE INGREDIENT | XHX3C3X673 | NUFLOR GOLD (FLORFENICOL) INJECTION [SCHERING CORPORATION] | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.