Package 71919-820-01

Brand: thiosinaminum

Generic: allylthiourea
NDC Package

Package Facts

Identity

Package NDC 71919-820-01
Digits Only 7191982001
Product NDC 71919-820
Description

350 PELLET in 1 VIAL, GLASS (71919-820-01)

Marketing

Marketing Status
Marketed Since 2023-11-08
Brand thiosinaminum
Generic allylthiourea
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cc89b36-a4aa-6cac-e063-6394a90a524f", "openfda": {"unii": ["706IDJ14B7"], "spl_set_id": ["09a6cc99-5ebd-5db7-e063-6294a90a80cf"], "manufacturer_name": ["Washington Homeopathic Products"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "350 PELLET in 1 VIAL, GLASS (71919-820-01)", "package_ndc": "71919-820-01", "marketing_start_date": "20231108"}], "brand_name": "Thiosinaminum", "product_id": "71919-820_2cc89b36-a4aa-6cac-e063-6394a90a524f", "dosage_form": "PELLET", "product_ndc": "71919-820", "generic_name": "ALLYLTHIOUREA", "labeler_name": "Washington Homeopathic Products", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thiosinaminum", "active_ingredients": [{"name": "ALLYLTHIOUREA", "strength": "200 [hp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20231108", "listing_expiration_date": "20261231"}