NDC 69626-0512-4 - Amerix Biotin
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
- 69626-0512
- Requested NDC
- 69626-0512-4
- Package NDCs from labels
- 69626-0512-4
- Manufacturer
- Leosons Overseas Corp | Smartscience Laboratories Inc.
- Effective date
- 2018-09-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Corn Syrup - Leosons Overseas Corp | Smartscience Laboratories Inc. | Leosons Overseas Corp | Smartscience Laboratories Inc. | 2018-09-13 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69626-0512-4 | Amerix Biotin | 60 in 1 BOTTLE | TABLET, CHEWABLE | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69626-0512 | AMERIX BIOTIN (BIOTIN) TABLET, CHEWABLE [LEOSONS OVERSEAS CORP] | 1 | 1 package rows | 20180914_8f0f2380-ebe3-480d-8a34-5a978950eded.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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.