NDC 58005-667 - Toxi-Sorb Bolus
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
- 58005-667
- Package NDCs from labels
- 58005-667-02
- Manufacturer
- Sparhawk Laboratories, Inc.
- Effective date
- 2014-04-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TOXI-SORB BOLUS | Sparhawk Laboratories, Inc. | 2014-04-29 | OTC ANIMAL DRUG LABEL |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ATTAPULGITE | ACTIVE INGREDIENT | U6V729APAM | TOXI-SORB BOLUS (ACTIVATED ATTAPULGITE) TABLET [SPARHAWK LABORATORIES, INC.] | 3 | |
| ATTAPULGITE | ACTIVE MOIETY | U6V729APAM | TOXI-SORB BOLUS (ACTIVATED ATTAPULGITE) TABLET [SPARHAWK LABORATORIES, INC.] | 3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.