NDC 57319-047 - Magnalax 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
- 57319-047
- Package NDCs from labels
- 57319-047-12
- Manufacturer
- Clipper Distributing Company, LLC | Sparhawk Laboratories, Inc.
- Effective date
- 2024-06-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Magnalax Bolus | Clipper Distributing Company, LLC | Sparhawk Laboratories, Inc. | 2024-06-06 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57319-047-12 | Magnalax Bolus | 50 in 1 BOX | TABLET | 50 | 1 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Zintrexyl-C | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb1492c5-bfca-d632-e053-2a95a90ad7d1 | 2023-01-11 | Warnings, Adverse reactions | 3A3U0GI71G |
| Magnesia Oxydata | MAGNESIA OXYDATA | Hahnemann Laboratories, INC. | e45bc2b0-72f4-42e1-e053-2995a90a0e66 | 2022-07-21 | 3A3U0GI71G | |
| Magnesium Oxide 400mg | MAGNESIUM OXIDE 400MG | Allegiant Health | 2ea68874-8c20-4284-bd0a-f07768057b83 | 2019-01-28 | Warnings | 3A3U0GI71G |
| Magnesium Oxide | MAGNESIUM OXIDE | Aphena Pharma Solutions - Tennessee, LLC | 11b2ce71-61fd-4e75-a859-a260b1dda080 | 2018-11-07 | Warnings | 3A3U0GI71G |
| Magnesium Oxide | MAGNESIUM OXIDE | Aphena Pharma Solutions - Tennessee, LLC | edabc9e4-60ad-407f-97c8-dfec5ee7eeb1 | 2018-10-25 | Warnings | 3A3U0GI71G |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.