Aconitum e tub. 30
- Product NDC
- 48951-9171
- 11-digit product format
- 489519171
- Labeler code
- 48951
- Product ID
- 48951-9171_c68ebe6c-88a0-12ee-e053-2a95a90a97e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum e tub. 30
- Dosage form
- LIQUID
- 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
- 30 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-9171 | ACONITUM E TUB. 30 LIQUID [URIEL PHARMACY INC.] | 6 | Legacy NDC | 20210708_8b80552a-6ae3-40ea-bf41-5cd705be04f2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-9171-1 | 48951917101 | 10 AMPULE in 1 BOX (48951-9171-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |