FDA.reportPublic FDA data

Chenopodium Anthelminticum

Product NDC
63545-475
11-digit product format
635450475
Labeler code
63545
Product ID
63545-475_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
6 [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
Chenopodium Anthelminticum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DYSPHANIA AMBROSIOIDES WHOLE6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4H5RSU087I

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-475-01Chenopodium Anthelminticum200 in 1 VIAL, GLASSPELLET2001
63545-475-02Chenopodium Anthelminticum1200 in 1 BOTTLE, GLASSPELLET12001
63545-475-03Chenopodium Anthelminticum4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-475CHENOPODIUM ANTHELMINTICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220512_dec35ba0-f611-0fa9-e053-2a95a90a0898.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63545-475-0163545047501200 PELLET in 1 VIAL, GLASS (63545-475-01) 200 pellet2022-05-110000-00-00NoNoCurrent
63545-475-02635450475021200 PELLET in 1 BOTTLE, GLASS (63545-475-02) 1200 pellet2022-05-110000-00-00NoNoCurrent
63545-475-03635450475034000 PELLET in 1 BOTTLE, GLASS (63545-475-03) 4000 pellet2022-05-110000-00-00NoNoCurrent