Antimonium tartaricum
- Product NDC
- 71919-829
- 11-digit product format
- 719190829
- Labeler code
- 71919
- Product ID
- 71919-829_3e89179f-2598-bca0-e063-6394a90a5b07
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ANTIMONY POTASSIUM TARTRATE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Washington Homeopathic Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-09-11
- Substance
- ANTIMONY POTASSIUM TARTRATE
- Active strength
- 30 [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Antimonium tartaricum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANTIMONY POTASSIUM TARTRATE | 30 [hp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | DL6OZ476V3 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71919-829-05 | Antimonium tartaricum | 900 in 1 VIAL, GLASS | PELLET | 900 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71919-829-05 | 71919082905 | 900 PELLET in 1 VIAL, GLASS (71919-829-05) | 900 pellet | 2025-09-11 | No | No | Historical |