Viscum Quercus
- Product NDC
- 48951-1006
- 11-digit product format
- 489511006
- Labeler code
- 48951
- Product ID
- 48951-1006_fe0e2f22-a395-433e-8ccb-db619c993ff9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- VISCUM ALBUM FRUITING TOP
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- VISCUM ALBUM FRUITING TOP
- Active strength
- 2 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 48951-1006-1 | Viscum Quercus | 1 mL in 1 AMPULE | LIQUID | 1 | | 1 |
| 48951-1006-1 | Viscum Quercus | 10 in 1 PACKAGE | LIQUID | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1006 | VISCUM QUERCUS (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC] | 1 | Legacy NDC, 2 package rows | 20130130_dbaa6477-6f07-43e9-90b9-ae8cf364628c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-1006-1 | 48951100601 | 1 mL in 1 AMPULE | 1 ml | Historical |