Bryonia
- Product NDC
- 44911-0382
- 11-digit product format
- 449110382
- Labeler code
- 44911
- Product ID
- 44911-0382_b5dfb385-847a-433b-a413-f8ad47616f8b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bryonia (Alba)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-08-19
- Substance
- BRYONIA ALBA ROOT
- Active strength
- 200 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bryonia
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BRYONIA ALBA ROOT | 200 [hp_C]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | T7J046YI2B |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 44911-0382-1 | Bryonia | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 44911-0382 | BRYONIA (BRYONIA (ALBA)) LIQUID [ENERGIQUE, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241027_f9a2b9f3-5e35-4c3a-a8ae-a7312118e4f0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0382-1 | 44911038201 | 30 mL in 1 BOTTLE, DROPPER (44911-0382-1) | 30 ml | 2016-08-19 | 0000-00-00 | No | No | Current |