NDC 37662-1644-01 - Dulcamara
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
- 37662-1644
- Requested NDC
- 37662-1644-01
- Package NDCs from labels
- 37662-1644-1, 37662-1644-2, 37662-1644-3, 37662-1644-4, 37662-1644-01
- Manufacturer
- Hahnemann Laboratories, INC.
- Effective date
- 2022-09-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dulcamara - Hahnemann Laboratories, INC. | Hahnemann Laboratories, INC. | 2022-09-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 37662-1644-1 | Dulcamara | 200 in 1 VIAL, GLASS | PELLET | 200 | 1 | |
| 37662-1644-2 | Dulcamara | 500 in 1 VIAL, GLASS | PELLET | 500 | 1 | |
| 37662-1644-3 | Dulcamara | 3000 in 1 BOTTLE, GLASS | PELLET | 3000 | 1 | |
| 37662-1644-4 | Dulcamara | 10000 in 1 BOTTLE, GLASS | PELLET | 10000 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 37662-1644 | DULCAMARA PELLET [HAHNEMANN LABORATORIES, INC.] | 1 | Current NDC, Legacy NDC, 4 package rows | 20221004_e9c7e259-dbae-271a-e053-2995a90aa178.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 |
|---|---|---|---|---|---|---|
| Anti Hive | AMMONIUM CARBONICUM, APIS MELLIFICA, ARGENTUM METALLICUM, ARSENICUM ALBUM, DULCAMARA, MEZEREUM, RHUS TOX, URTICA URENS | BioActive Nutritional, Inc. | e3f87bf5-91a3-4674-ae8f-1f84c8ef579b | 2017-03-30 | Warnings | KPS1B1162N |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.