Package 0220-4971-41

Brand: thiosinaminum

Generic: allylthiourea
NDC Package

Package Facts

Identity

Package NDC 0220-4971-41
Digits Only 0220497141
Product NDC 0220-4971
Product ID 0220-4971_f2f5c1ee-8932-321c-e053-2995a90a2717
Description

30 [hp_C] in 1 TUBE (0220-4971-41)

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": "f2f5c1ee-8932-321c-e053-2995a90a2717", "openfda": {"unii": ["706IDJ14B7"], "spl_set_id": ["86590806-9e23-d0f5-e053-2991aa0a14ea"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-4971-41)", "package_ndc": "0220-4971-41", "marketing_start_date": "19830303"}], "brand_name": "Thiosinaminum", "product_id": "0220-4971_f2f5c1ee-8932-321c-e053-2995a90a2717", "dosage_form": "PELLET", "product_ndc": "0220-4971", "generic_name": "ALLYLTHIOUREA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thiosinaminum", "active_ingredients": [{"name": "ALLYLTHIOUREA", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}