Stannum Succinum
- Product NDC
- 48951-8365
- Requested package NDC
- 48951-8365-1
- 11-digit product format
- 489518365
- Labeler code
- 48951
- Product ID
- 48951-8365_b70f7b60-4239-11be-e053-2a95a90a49fb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stannum Succinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- AMBER; TIN
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 48951-8365-1 | Stannum Succinum | 1 in 1 BAG | LIQUID | 1 | | 7 |
| 48951-8365-1 | Stannum Succinum | 10 mL in 1 BOTTLE, DROPPER | LIQUID | 10 | | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8365 | STANNUM SUCCINUM LIQUID [URIEL PHARMACY INC.] | 7 | Legacy NDC, 2 package rows | 20240328_c8b6c6eb-abc1-4390-85f4-e7a7d08f63e4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8365-1 | 48951836501 | 1 BOTTLE, DROPPER in 1 BAG (48951-8365-1) > 10 mL in 1 BOTTLE, DROPPER | 2009-09-01 | 0000-00-00 | No | No | Current |