NDC 59517-1730 - Stop 20-pm
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
- 59517-1730
- Package NDCs from labels
- 59517-1730-4
- Manufacturer
- Immuvet, Inc. | Amino Cell, Inc
- Effective date
- 2025-10-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Stop 20-pm - Immuvet, Inc. | Amino Cell, Inc | Immuvet, Inc. | Amino Cell, Inc | 2025-10-06 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59517-1730-4 | Stop 20-pm | 200 mL in 1 BOTTLE | LIQUID | 200 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59517-1730 | STOP 20-PM (ANTIMONY POTASSIUM TARTRATE, ACONITUM NAPELLUS, PHOSPHORUS, POTASSIUM CARBONATE, MERCURIUS SOLUBILIS, BRYONIA ALBA, PARIS QUADRIFOLIA) LIQUID [IMMUVET, INC.] | 1 | 1 package rows | 20220831_4112da8c-b3b4-4d34-86b7-17e98d054cd3.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.