Home NDC 0220-5049 Trillium pendulum
Product NDC 0220-5049
11-digit product format 002205049
Labeler code 0220
Product ID 0220-5049_00edbc51-9a8b-566f-e063-6294a90a81a7
Type HUMAN OTC DRUG
Nonproprietary name TRILLIUM ERECTUM ROOT
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance TRILLIUM ERECTUM ROOT
Active strength 9 [hp_C]/9[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 Trillium pendulum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRILLIUM ERECTUM ROOT 9 [hp_C]/9[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination AHW6F0T2X0 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-5049-41 Trillium pendulum 9 [hp_C] in 1 TUBE PELLET 9 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-5049 TRILLIUM PENDULUM (TRILLIUM ERECTUM ROOT) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20230721_813f27b2-02e8-f7ae-e053-2a91aa0a7409.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 0220-5049-41 00220504941 9 [hp_C] in 1 TUBE (0220-5049-41) 1983-03-03 0000-00-00 No No Current