Bryonia Alba
- Product NDC
- 57471-3061
- 11-digit product format
- 574713061
- Labeler code
- 57471
- Product ID
- 57471-3061_5d48ea4c-f49e-4ce3-b126-589bece4170a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bryonia Alba
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Celletech Ltd.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1988-07-01
- Marketing end
- 0000-00-00
- Substance
- BRYONIA ALBA ROOT
- Active strength
- 30 [hp_C]/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 57471-3061-3 | Bryonia Alba | 800 in 1 BOTTLE | PELLET | 800 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57471-3061 | BRYONIA ALBA PELLET [CELLETECH LTD.] | 1 | Legacy NDC, 1 package rows | 20120908_4e21f8cd-0f69-4212-90b5-feab349b64bf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 57471-3061-3 | 57471306103 | 800 in 1 BOTTLE | Historical |