Aconite
- Product NDC
- 44911-0152
- 11-digit product format
- 449110152
- Labeler code
- 44911
- Product ID
- 44911-0152_5ef452e3-1085-4a79-a8ba-3eb7a1d2be7a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-05-14
- Marketing end
- 2022-09-20
- Substance
- ACONITUM NAPELLUS
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0152-1 | 44911015201 | 30 mL in 1 BOTTLE, DROPPER (44911-0152-1) | 30 ml | 2015-05-14 | 2022-09-20 | No | No | Current |