FDA.reportPublic FDA data

Scandium Oxydatum

Product NDC
37662-2992
11-digit product format
376622992
Labeler code
37662
Product ID
37662-2992_f9d0b7ba-bf4d-fe21-e053-6394a90a0621
Type
HUMAN OTC DRUG
Nonproprietary name
Scandium Oxydatum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-04-20
Substance
SCANDIUM OXIDE
Active strength
100 [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
Scandium Oxydatum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SCANDIUM OXIDE100 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiT0G94L07ZD

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2992-1Scandium Oxydatum200 in 1 VIAL, GLASSPELLET2001
37662-2992-2Scandium Oxydatum500 in 1 VIAL, GLASSPELLET5001
37662-2992-3Scandium Oxydatum3000 in 1 BOTTLE, GLASSPELLET30001
37662-2992-4Scandium Oxydatum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2992SCANDIUM OXYDATUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230421_f9d0b7ba-bf4c-fe21-e053-6394a90a0621.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2992-137662299201200 PELLET in 1 VIAL, GLASS (37662-2992-1) 200 pellet2023-04-20NoNoCurrent
37662-2992-237662299202500 PELLET in 1 VIAL, GLASS (37662-2992-2) 500 pellet2023-04-20NoNoCurrent
37662-2992-3376622992033000 PELLET in 1 BOTTLE, GLASS (37662-2992-3) 3000 pellet2023-04-20NoNoCurrent
37662-2992-43766229920410000 PELLET in 1 BOTTLE, GLASS (37662-2992-4) 10000 pellet2023-04-20NoNoCurrent