Veratrum Alb
- Product NDC
- 44911-0395
- 11-digit product format
- 449110395
- Labeler code
- 44911
- Product ID
- 44911-0395_d76e019d-21b8-4ab8-9d8a-690870b85b2f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Veratrum Album
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-08-23
- Marketing end
- 2022-08-16
- Substance
- VERATRUM ALBUM ROOT
- Active strength
- 200 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0395-1 | 44911039501 | 30 mL in 1 BOTTLE, DROPPER (44911-0395-1) | 30 ml | 2016-08-23 | 0000-00-00 | No | No | Current |