Viscum (I) Quercus Series 0
- Product NDC
- 48951-9083
- 11-digit product format
- 489519083
- Labeler code
- 48951
- Product ID
- 48951-9083_8b4ea9ed-b277-4f07-9ff2-07c9ee74242b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Viscum (I) Quercus Series 0
- 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
- 3 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-9083-1 | Viscum (I) Quercus Series 0 | 1 mL in 1 AMPULE | LIQUID | 1 | | 1 |
| 48951-9083-1 | Viscum (I) Quercus Series 0 | 10 in 1 BOX | LIQUID | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-9083 | VISCUM (I) QUERCUS SERIES 0 LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 2 package rows | 20150127_1b0a231b-cc61-402e-9c05-154da5d06d44.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-9083-1 | 48951908301 | 1 mL in 1 AMPULE | 1 ml | Historical |