Stannum 21X
- Product NDC
- 48951-8361
- 11-digit product format
- 489518361
- Labeler code
- 48951
- Product ID
- 48951-8361_4886865e-c543-7b22-e063-6394a90a6f14
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stannum 21X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- TIN
- Active strength
- 21 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Stannum 21X
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TIN | 21 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 387GMG9FH5 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8361-1 | Stannum 21X | 1 mL in 1 AMPULE | LIQUID | 1 | | 2 |
| 48951-8361-1 | Stannum 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 |
|---|
| 48951-8361 | STANNUM 21X LIQUID [URIEL PHARMACY INC.] | 1 | Current NDC, Legacy NDC, 2 package rows | 20191106_969cb4b7-c1c2-0577-e053-2a95a90a4e2c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8361-1 | 48951836101 | 10 AMPULE in 1 BOX (48951-8361-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |