Abrotanum
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Abrotanum
- Generic name
- ABROTANUM
- Manufacturer
- Hahnemann Laboratories, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 99ef26d5-de23-1cae-e053-2995a90a3ffd
- SPL ID
- 2b4a1f65-5ba7-16e6-e063-6394a90afb58
- Version
- 10
- Effective date
- 2025-01-09
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:51:01
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Abrotanum | openfda.brand_name | |
| generic name | ABROTANUM | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, Inc. | openfda.manufacturer_name | |
| ndc | package | 63545-713-04 | openfda.package_ndc |
| ndc | product | 63545-713 | openfda.product_ndc |
| ndc11 | package | 63545071304 | derived:openfda.package_ndc |
| spl id | 2b4a1f65-5ba7-16e6-e063-6394a90afb58 | id | |
| spl set id | 99ef26d5-de23-1cae-e053-2995a90a3ffd | set_id | |
| unii | QG07G580U0 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.