NDC 58198-0035-2 - Loncor 300
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
- 58198-0035
- Requested NDC
- 58198-0035-2
- Package NDCs from labels
- 58198-0035-2, 58198-0035-1, 58198-0035-3
- Manufacturer
- Elanco US Inc.
- Effective date
- 2023-11-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Elanco ™ Loncor™ 300 (florfenicol) 300 mg/mL Injectable Solution | Elanco US Inc. | 2023-11-27 | PRESCRIPTION ANIMAL DRUG LABEL |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.