NDC 54925-035-37 - SULFASOL
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
- 54925-035
- Requested NDC
- 54925-035-37
- Package NDCs from labels
- 54925-035-37
- Manufacturer
- Med-Pharmex, Inc
- Effective date
- 2023-06-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SULFASOL - Med-Pharmex, Inc | Med-Pharmex, Inc | 2023-06-23 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| SULFADIMETHOXINE SODIUM | ACTIVE INGREDIENT | 49DG2B481W | SULFASOL (SULFADIMETHOXINE SODIUM) POWDER, FOR SOLUTION [MED-PHARMEX, INC] | 1 | |
| SULFADIMETHOXINE | ACTIVE MOIETY | 30CPC5LDEX | SULFASOL (SULFADIMETHOXINE SODIUM) POWDER, FOR SOLUTION [MED-PHARMEX, INC] | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.