Apis Aconitum
- Product NDC
- 48951-1042
- 11-digit product format
- 489511042
- Labeler code
- 48951
- Product ID
- 48951-1042_9842561e-c79f-fa31-e053-2a95a90aa90f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Apis Aconitum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- APIS MELLIFERA; ATROPA BELLADONNA; ACONITUM NAPELLUS
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1042-3 | Apis Aconitum | 30 mL in 1 BOTTLE, GLASS | LIQUID | 30 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1042 | APIS ACONITUM LIQUID [URIEL PHARMACY INC.] | 3 | Legacy NDC, 1 package rows | 20191127_f2ed7d2a-b69b-4e84-a0e0-4975ef0698b8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1042-3 | 48951104203 | 30 mL in 1 BOTTLE, GLASS (48951-1042-3) | 30 ml | 2009-09-01 | 0000-00-00 | No | No | Current |