FDA.reportPublic FDA data

Thiosinaminum

Product NDC
37662-2306
11-digit product format
376622306
Labeler code
37662
Product ID
37662-2306_f1f61f7e-bb41-4ee8-e053-2a95a90a08bd
Type
HUMAN OTC DRUG
Nonproprietary name
Thiosinaminum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-01-11
Substance
ALLYLTHIOUREA
Active strength
12 [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
Thiosinaminum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALLYLTHIOUREA12 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii706IDJ14B7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2306-1Thiosinaminum200 in 1 VIAL, GLASSPELLET2001
37662-2306-2Thiosinaminum1200 in 1 BOTTLE, GLASSPELLET12001
37662-2306-3Thiosinaminum4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2306THIOSINAMINUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20230112_f1f61f7e-bb40-4ee8-e053-2a95a90a08bd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-2306-137662230601200 PELLET in 1 VIAL, GLASS (37662-2306-1) 200 pellet2023-01-110000-00-00NoNoCurrent
37662-2306-2376622306021200 PELLET in 1 BOTTLE, GLASS (37662-2306-2) 1200 pellet2023-01-110000-00-00NoNoCurrent
37662-2306-3376622306034000 PELLET in 1 BOTTLE, GLASS (37662-2306-3) 4000 pellet2023-01-110000-00-00NoNoCurrent