NDC 75839-235-10 - CLENBUTEROL HYDROCHLORIDE
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
- 75839-235
- Requested NDC
- 75839-235-10
- Package NDCs from labels
- 75839-235-10, 75839-235-05
- Manufacturer
- Attix Pharmaceuticals
- Effective date
- 2019-10-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CLENBUTEROL HYDROCHLORIDE - Attix Pharmaceuticals | Attix Pharmaceuticals | 2019-10-30 | BULK INGREDIENT |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CLENBUTEROL HYDROCHLORIDE | ACTIVE INGREDIENT | GOR5747GWU | CLENBUTEROL HYDROCHLORIDE (CLENBUTEROL HCL) POWDER [ATTIX PHARMACEUTICALS] | 2 | |
| CLENBUTEROL | ACTIVE MOIETY | XTZ6AXU7KN | CLENBUTEROL HYDROCHLORIDE (CLENBUTEROL HCL) POWDER [ATTIX PHARMACEUTICALS] | 2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.