Home NDC 0220-0379 Antimonium tartaricum
Product NDC 0220-0379
11-digit product format 002200379
Labeler code 0220
Product ID 0220-0379_0d08468e-40e0-174c-e063-6394a90ac3f7
Type HUMAN OTC DRUG
Nonproprietary name ANTIMONY POTASSIUM TARTRATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance ANTIMONY POTASSIUM TARTRATE
Active strength 12 [hp_C]/12[hp_C]
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 12 [hp_C]/12[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination DL6OZ476V3 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-0379-41 Antimonium tartaricum 12 [hp_C] in 1 TUBE PELLET 12 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0379 ANTIMONIUM TARTARICUM (ANTIMONY POTASSIUM TARTRATE ) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20231222_845faacc-2532-d99e-e053-2991aa0a5b85.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0220-0379-41 00220037941 12 [hp_C] in 1 TUBE (0220-0379-41) 1983-03-03 0000-00-00 No No Current