ANTIMONIUM TARTARICUM
- Product NDC
- 10191-1844
- 11-digit product format
- 101911844
- Labeler code
- 10191
- Product ID
- 10191-1844_303af7ac-5b7c-48de-b9a2-a3040f50c965
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ANTIMONY POTASSIUM TARTRATE
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2004-10-11
- Marketing end
- 0000-00-00
- Substance
- ANTIMONY POTASSIUM TARTRATE
- Active strength
- 15 [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 |
|---|
| 10191-1844-2 | ANTIMONIUM TARTARICUM | 151 in 1 VIAL, GLASS | PELLET | 151 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1844 | ANTIMONIUM TARTARICUM (ANTIMONY POTASSIUM TARTRATE) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20100625_394652a8-e0cc-4530-b2a5-5df8b19e3fa1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1844-2 | 10191184402 | 151 in 1 VIAL, GLASS | Historical |