Package 0220-0418-41

Brand: antimonium iodatum

Generic: antimony triiodide
NDC Package

Package Facts

Identity

Package NDC 0220-0418-41
Digits Only 0220041841
Product NDC 0220-0418
Description

200 [kp_C] in 1 TUBE (0220-0418-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand antimonium iodatum
Generic antimony triiodide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "141d6037-8729-bc6c-e063-6294a90a475c", "openfda": {"unii": ["52ZE5Y9Y82"], "spl_set_id": ["141d6037-8728-bc6c-e063-6294a90a475c"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0418-41)", "package_ndc": "0220-0418-41", "marketing_start_date": "20240101"}], "brand_name": "Antimonium iodatum", "product_id": "0220-0418_141d6037-8729-bc6c-e063-6294a90a475c", "dosage_form": "PELLET", "product_ndc": "0220-0418", "generic_name": "ANTIMONY TRIIODIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antimonium iodatum", "active_ingredients": [{"name": "ANTIMONY TRIIODIDE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}