Package 0220-4972-41

Brand: thiosinaminum

Generic: allylthiourea
NDC Package

Package Facts

Identity

Package NDC 0220-4972-41
Digits Only 0220497241
Product NDC 0220-4972
Product ID 0220-4972_0a34b653-86a5-787d-e063-6394a90a1970
Description

200 [kp_C] in 1 TUBE (0220-4972-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand thiosinaminum
Generic allylthiourea
Sample Package No

Linked Drug Pages (1)

Thiosinaminum ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a34b653-86a5-787d-e063-6394a90a1970", "openfda": {"unii": ["706IDJ14B7"], "spl_set_id": ["86590806-9e0c-d0f5-e053-2991aa0a14ea"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-4972-41)", "package_ndc": "0220-4972-41", "marketing_start_date": "19830303"}], "brand_name": "Thiosinaminum", "product_id": "0220-4972_0a34b653-86a5-787d-e063-6394a90a1970", "dosage_form": "PELLET", "product_ndc": "0220-4972", "generic_name": "ALLYLTHIOUREA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thiosinaminum", "active_ingredients": [{"name": "ALLYLTHIOUREA", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}