Aconitum napellus
- Product NDC
- 0220-0050
- 11-digit product format
- 002200050
- Labeler code
- 0220
- Product ID
- 0220-0050_b3373450-fc02-8ba4-e053-2a95a90aa31e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACONITUM NAPELLUS
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Laboratoires Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS
- Active strength
- 3 [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 0220-0050 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 0220-0050 | 0220-0050-41 | D | Discontinued by firm | 2026-07-31 |