thiosinaminum

Generic: thiosinaminum

Labeler: hahnemann laboratories, inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name thiosinaminum
Generic Name thiosinaminum
Labeler hahnemann laboratories, inc.
Dosage Form PELLET
Routes
ORAL
Active Ingredients

allylthiourea 1 [hp_Q]/1

Manufacturer
Hahnemann Laboratories, INC.

Identifiers & Regulatory

Product NDC 37662-2312
Product ID 37662-2312_f1f61f7e-bb41-4ee8-e053-2a95a90a08bd
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2023-01-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 376622312
Hyphenated Format 37662-2312

Supplemental Identifiers

UNII
706IDJ14B7

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name thiosinaminum (source: ndc)
Generic Name thiosinaminum (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 [hp_Q]/1
source: ndc
Packaging
  • 10000 PELLET in 1 BOTTLE, GLASS (37662-2312-1)
source: ndc

Packages (1)

37662-2312-1 10000 PELLET in 1 BOTTLE, GLASS (37662-2312-1)

Ingredients (1)

allylthiourea (1 [hp_Q]/1)

Linked Drug Pages (1)

Thiosinaminum ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f1f61f7e-bb41-4ee8-e053-2a95a90a08bd", "openfda": {"unii": ["706IDJ14B7"], "spl_set_id": ["f1f61f7e-bb40-4ee8-e053-2a95a90a08bd"], "manufacturer_name": ["Hahnemann Laboratories, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10000 PELLET in 1 BOTTLE, GLASS (37662-2312-1)", "package_ndc": "37662-2312-1", "marketing_start_date": "20230111"}], "brand_name": "Thiosinaminum", "product_id": "37662-2312_f1f61f7e-bb41-4ee8-e053-2a95a90a08bd", "dosage_form": "PELLET", "product_ndc": "37662-2312", "generic_name": "Thiosinaminum", "labeler_name": "Hahnemann Laboratories, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thiosinaminum", "active_ingredients": [{"name": "ALLYLTHIOUREA", "strength": "1 [hp_Q]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20230111", "listing_expiration_date": "20261231"}