Aconitum
- Product NDC
- 53645-1610
- 11-digit product format
- 536451610
- Labeler code
- 53645
- Product ID
- 53645-1610_f0312815-fc62-1ff3-e053-2995a90ac4c4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-11-24
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS ROOT
- Active strength
- 30 [hp_X]/23g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53645-1610 | ACONITUM GLOBULE [TRUE BOTANICA, LLC] | 5 | Legacy NDC | 20230502_61870547-8bb3-35ff-e053-2a91aa0a2a50.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53645-1610-2 | 53645161002 | 23 g in 1 BOTTLE (53645-1610-2) | 23 g | 2017-11-24 | 0000-00-00 | No | No | Current |