Viscum Pini 50
- Product NDC
- 48951-9320
- Requested package NDC
- 48951-9320-1
- 11-digit product format
- 489519320
- Labeler code
- 48951
- Product ID
- 48951-9320_6bf092e6-8c25-3b51-e053-2991aa0ad8b2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Viscum Pini 50
- 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
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-9320-1 | Viscum Pini 50 | 8 in 1 BOX | LIQUID | 8 | | 5 |
| 48951-9320-1 | Viscum Pini 50 | 1 mL in 1 AMPULE | LIQUID | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-9320 | VISCUM PINI 50 LIQUID [URIEL PHARMACY INC.] | 5 | Legacy NDC, 2 package rows | 20241206_f19bb083-7fa8-4689-abdc-6f2a2a6f0fe4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-9320-1 | 48951932001 | 8 AMPULE in 1 BOX (48951-9320-1) > 1 mL in 1 AMPULE | 8 ampule | 2014-08-01 | 0000-00-00 | No | No | Current |