Stibium 20X
- Product NDC
- 48951-8410
- 11-digit product format
- 489518410
- Labeler code
- 48951
- Product ID
- 48951-8410_4e440513-3fe9-ad73-e063-6294a90a0428
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stibium 20X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- ANTIMONY
- Active strength
- 20 [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
- Stibium 20X
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANTIMONY | 20 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9IT35J3UV3 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8410-3 | Stibium 20X | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8410 | STIBIUM 20X LIQUID [URIEL PHARMACY INC.] | 1 | Current NDC, 1 package rows | 20240319_13f25caf-51f0-6b2f-e063-6394a90a0920.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-8410-3 | 48951841003 | 60 mL in 1 BOTTLE, DROPPER (48951-8410-3) | 60 ml | 2009-09-01 | No | No | Historical |