NDC 86024-009-00 - FISH FLOX FORTE
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
- 86024-009
- Requested NDC
- 86024-009-00
- Package NDCs from labels
- 86024-009-30, 86024-009-00, 86024-009-12
- Manufacturer
- Thomas Labs, LLC | Aurobindo Pharma Limited
- Effective date
- 2017-01-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FISH FLOX FORTE - Thomas Labs, LLC | Aurobindo Pharma Limited | Thomas Labs, LLC | Aurobindo Pharma Limited | 2017-01-31 | OTC ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CIPROFLOXACIN | ACTIVE INGREDIENT | 5E8K9I0O4U | FISH FLOX FORTE (CIPROFLOXACIN) TABLET, FILM COATED [THOMAS LABS, LLC] | 2 | |
| CIPROFLOXACIN | ACTIVE MOIETY | 5E8K9I0O4U | FISH FLOX FORTE (CIPROFLOXACIN) TABLET, FILM COATED [THOMAS LABS, LLC] | 2 |
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 |
|---|---|---|---|---|---|---|
| Ciprofloxacin | CIPROFLOXACIN | Sagent Pharmaceuticals | f406e796-17d9-4465-b8a7-00d966a4ba74 | 2026-08-04 | Boxed warning, Warnings, Adverse reactions | 5E8K9I0O4U |
| Ciprofloxacin in Dextrose | CIPROFLOXACIN | ProPharma Distribution | 42c758be-4d44-018a-e063-6294a90ae041 | 2025-11-04 | Boxed warning, Warnings, Adverse reactions | 5E8K9I0O4U |
| Ciprofloxacin in Dextrose | CIPROFLOXACIN | Hospira, Inc. | cbbbf939-3219-4515-a48e-ca264daa4d07 | 2025-11-04 | Boxed warning, Warnings, Adverse reactions | 5E8K9I0O4U |
| Ciprofloxacin | CIPROFLOXACIN | Sagent Pharmaceuticals | 7049f870-6741-4a67-8033-398c36126a06 | 2022-09-19 | Boxed warning, Warnings, Adverse reactions | 5E8K9I0O4U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.