Package 0220-0418-41
Brand: antimonium iodatum
Generic: antimony triiodidePackage 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
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"}