Aconitum e tub. 6
- Product NDC
- 48951-1009
- 11-digit product format
- 489511009
- Labeler code
- 48951
- Product ID
- 48951-1009_6d858b0e-a3cb-2686-e053-2991aa0acc06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum e tub. 6
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS
- Active strength
- 6 [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 | 48951-1009 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 48951-1009 | 48951-1009-2 | D | Discontinued by firm | 2026-07-31 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ACONITUM NAPELLUS | ACTIVE INGREDIENT | U0NQ8555JD | ACONITUM E TUB. 6 PELLET [URIEL PHARMACY INC.] | 1 | |
| ACONITUM NAPELLUS | ACTIVE MOIETY | U0NQ8555JD | ACONITUM E TUB. 6 PELLET [URIEL PHARMACY INC.] | 1 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | ACONITUM E TUB. 6 PELLET [URIEL PHARMACY INC.] | 1 |