NDC 72969-117-10 - OXIBENDAZOLE
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
- 72969-117
- Requested NDC
- 72969-117-10
- Package NDCs from labels
- 72969-117-10
- Manufacturer
- PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
- Effective date
- 2021-12-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OXIBENDAZOLE - PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC | PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC | 2021-12-21 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72969-117-10 | OXIBENDAZOLE | 1 g in 1 PACKAGE | POWDER | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.