Argentum 21X
- Product NDC
- 48951-1328
- 11-digit product format
- 489511328
- Labeler code
- 48951
- Product ID
- 48951-1328_969c0200-c8a6-0517-e053-2a95a90aa264
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Argentum 21X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-11-05
- Marketing end
- 0000-00-00
- Substance
- SILVER
- Active strength
- 21 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 48951-1328-1 | Argentum 21X | 1 mL in 1 AMPULE | LIQUID | 1 | | 2 |
| 48951-1328-1 | Argentum 21X | 10 in 1 BOX | LIQUID | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1328 | ARGENTUM 21X LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 2 package rows | 20240402_969c0200-c8a5-0517-e053-2a95a90aa264.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1328-1 | 48951132801 | 10 AMPULE in 1 BOX (48951-1328-1) > 1 mL in 1 AMPULE | 10 ampule | 2019-11-05 | 0000-00-00 | No | No | Current |