Aconitum Bryonia
- Product NDC
- 48951-1359
- 11-digit product format
- 489511359
- Labeler code
- 48951
- Product ID
- 48951-1359_ed38a70c-9874-8823-e053-2a95a90aad06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Bryonia
- 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; BRYONIA ALBA ROOT
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1359-3 | Aconitum Bryonia | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1359 | ACONITUM BRYONIA LIQUID [URIEL PHARMACY, INC.] | 2 | Legacy NDC, 1 package rows | 20241225_ed38a70c-9873-8823-e053-2a95a90aad06.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1359-3 | 48951135903 | 60 mL in 1 BOTTLE, DROPPER (48951-1359-3) | 60 ml | 2009-09-01 | 0000-00-00 | No | No | Current |