NDC 75839-810-50 - CISAPRIDE MONOHYDRATE
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
- 75839-810
- Requested NDC
- 75839-810-50
- Package NDCs from labels
- 75839-810-00, 75839-810-01, 75839-810-05, 75839-810-25, 75839-810-02, 75839-810-10, 75839-810-11, 75839-810-50
- Manufacturer
- Attix Pharmaceuticals Inc
- Effective date
- 2019-10-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CISAPRIDE MONOHYDRATE - Attix Pharmaceuticals Inc | Attix Pharmaceuticals Inc | 2019-10-30 | BULK INGREDIENT |
| Cisapride Monohydrate - Attix Pharmaceuticals | Attix Pharmaceuticals | 2017-03-27 | BULK INGREDIENT |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CISAPRIDE MONOHYDRATE | ACTIVE INGREDIENT | VZV0A4I38W | CISAPRIDE MONOHYDRATE POWDER [ATTIX PHARMACEUTICALS] | 2 | |
| CISAPRIDE | ACTIVE MOIETY | UVL329170W | CISAPRIDE MONOHYDRATE POWDER [ATTIX PHARMACEUTICALS] | 2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.