ANTIMONIUM TARTARICUM
- Product NDC
- 10191-1841
- 11-digit product format
- 101911841
- Labeler code
- 10191
- Product ID
- 10191-1841_e952cbaa-1420-49af-8d3c-a05c704c46a9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ANTIMONY POTASSIUM TARTRATE
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-01-06
- Marketing end
- 0000-00-00
- Substance
- ANTIMONY POTASSIUM TARTRATE
- Active strength
- 6 [hp_C]/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10191-1841-2 | ANTIMONIUM TARTARICUM | 176 in 1 VIAL, GLASS | PELLET | 176 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1841 | ANTIMONIUM TARTARICUM (ANTIMONY POTASSIUM TARTRATE) PELLET [REMEDY MAKERS] | 4 | Legacy NDC, 1 package rows | 20100212_7f1ec4ad-3605-4539-b52f-f03301b42ced.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1841-2 | 10191184102 | 176 in 1 VIAL, GLASS | Historical |