NDC 0859-2266-02 - Rompun
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
- 0859-2266
- Requested NDC
- 0859-2266-02
- Package NDCs from labels
- 0859-2266-02, 0859-2266-01
- Manufacturer
- Bayer HealthCare, LLC
- Effective date
- 2021-11-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rompun - Bayer HealthCare, LLC | Bayer HealthCare, LLC | 2021-11-09 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| XYLAZINE | ACTIVE INGREDIENT | 2KFG9TP5V8 | ROMPUN (XYLAZINE) INJECTION, SOLUTION [BAYER HEALTHCARE, LLC] | 3 | |
| XYLAZINE | ACTIVE MOIETY | 2KFG9TP5V8 | ROMPUN (XYLAZINE) INJECTION, SOLUTION [BAYER HEALTHCARE, LLC] | 3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.