Home NDC 63545-479-02 Chenopodium Anthelminticum
Product NDC 63545-479
Requested package NDC 63545-479-02
11-digit product format 635450479
Labeler code 63545
Product ID 63545-479_dec35ba0-f612-0fa9-e053-2a95a90a0898
Type HUMAN OTC DRUG
Nonproprietary name Chenopodium Anthelminticum
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-05-11
Substance DYSPHANIA AMBROSIOIDES WHOLE
Active strength 200 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Chenopodium Anthelminticum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DYSPHANIA AMBROSIOIDES WHOLE 200 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4H5RSU087I 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 63545-479-01 Chenopodium Anthelminticum 200 in 1 VIAL, GLASS PELLET 200 1 63545-479-02 Chenopodium Anthelminticum 500 in 1 VIAL, GLASS PELLET 500 1 63545-479-03 Chenopodium Anthelminticum 3000 in 1 BOTTLE, GLASS PELLET 3000 1 63545-479-04 Chenopodium Anthelminticum 10000 in 1 BOTTLE, GLASS PELLET 10000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63545-479 CHENOPODIUM ANTHELMINTICUM PELLET [HAHNEMANN LABORATORIES, INC.] 1 Current NDC, Legacy NDC, 4 package rows 20220512_dec35ba0-f611-0fa9-e053-2a95a90a0898.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 Units Marketing start Marketing end Sample Exclude flag Status 63545-479-02 63545047902 500 PELLET in 1 VIAL, GLASS (63545-479-02) 500 pellet 2022-05-11 0000-00-00 No No Current