NDC 55999-089-12 - Kanaplex
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
- 55999-089
- Requested NDC
- 55999-089-12
- Package NDCs from labels
- 55999-089-12, 55999-089-57, 55999-089-56, 55999-089-15, 55999-089-18
- Manufacturer
- Seachem Laboratories Inc.
- Effective date
- 2018-07-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Kanaplex™ | Seachem Laboratories Inc. | 2018-07-13 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55999-089-12 | Kanaplex | 5 g in 1 VIAL, PLASTIC | POWDER | 5 | 1 | |
| 55999-089-15 | Kanaplex | 100 g in 1 VIAL, PLASTIC | POWDER | 100 | 1 | |
| 55999-089-18 | Kanaplex | 1000 g in 1 VIAL, PLASTIC | POWDER | 1000 | 1 | |
| 55999-089-56 | Kanaplex | 6 in 1 CASE | POWDER | 6 | 1 | |
| 55999-089-57 | Kanaplex | 1 in 1 CARTON | POWDER | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.