Cuprum 21X
- Product NDC
- 48951-3233
- 11-digit product format
- 489513233
- Labeler code
- 48951
- Product ID
- 48951-3233_99496bc5-bd8d-7ca4-e053-2995a90a7bc0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cuprum 21X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- COPPER
- Active strength
- 21 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 48951-3233-1 | Cuprum 21X | 1 mL in 1 AMPULE | LIQUID | 1 | | 1 |
| 48951-3233-1 | Cuprum 21X | 10 in 1 BOX | LIQUID | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-3233 | CUPRUM 21X LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 2 package rows | 20191210_99496bc5-bd8c-7ca4-e053-2995a90a7bc0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-3233-1 | 48951323301 | 10 AMPULE in 1 BOX (48951-3233-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |