ANTIMONIUM TARTARICUM
- Product NDC
- 10191-1842
- 11-digit product format
- 101911842
- Labeler code
- 10191
- Product ID
- 10191-1842_1c8ee4c3-f0df-4bfe-aa6a-6e6857dfcb44
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antimony Potassium Tartrate
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2002-09-09
- Marketing end
- 0000-00-00
- Substance
- ANTIMONY POTASSIUM TARTRATE
- Active strength
- 9 [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 |
|---|
| 10191-1842-2 | ANTIMONIUM TARTARICUM | 169 in 1 VIAL, GLASS | PELLET | 169 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1842 | ANTIMONIUM TARTARICUM (ANTIMONY POTASSIUM TARTRATE) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20100621_b2377f87-7605-4b9e-b0f3-4fb81f263da0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1842-2 | 10191184202 | 169 in 1 VIAL, GLASS | Historical |