NDC 37662-3660-01 - Anacardium Orientale
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
- 37662-3660
- Requested NDC
- 37662-3660-01
- Package NDCs from labels
- 37662-3660-1, 37662-3660-2, 37662-3660-3, 37662-3660-4, 37662-3660-01
- Manufacturer
- Hahnemann Laboratories, INC.
- Effective date
- 2023-08-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Anacardium Orientale - Hahnemann Laboratories, INC. | Hahnemann Laboratories, INC. | 2023-08-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 37662-3660-1 | Anacardium Orientale | 200 in 1 VIAL, GLASS | PELLET | 200 | 1 | |
| 37662-3660-2 | Anacardium Orientale | 500 in 1 VIAL, GLASS | PELLET | 500 | 1 | |
| 37662-3660-3 | Anacardium Orientale | 3000 in 1 BOTTLE, GLASS | PELLET | 3000 | 1 | |
| 37662-3660-4 | Anacardium Orientale | 10000 in 1 BOTTLE, GLASS | PELLET | 10000 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 37662-3660 | ANACARDIUM ORIENTALE PELLET [HAHNEMANN LABORATORIES, INC.] | 1 | Current NDC, 4 package rows | 20230802_01e691d3-858c-f907-e063-6294a90a5d38.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Senility HP | ANACARDIUM ORIENTALE, BELLADONNA, HYOSCYAMUS NIGER, VERATRUM ALBUM, BARYTA CARBONICA, LACHESIS MUTUS, PHOSPHORUS, STRAMONIUM | BioActive Nutritional, Inc. | 214cf942-5277-4f4b-af7d-a9fcc6c8bd37 | 2017-02-23 | Warnings | Y0F0BU8RDU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.