Package 0220-5031-41

Brand: titanium metallicum

Generic: titanium
NDC Package

Package Facts

Identity

Package NDC 0220-5031-41
Digits Only 0220503141
Product NDC 0220-5031
Description

200 [kp_C] in 1 TUBE (0220-5031-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand titanium metallicum
Generic titanium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21b504bc-e12e-3a8e-e063-6294a90a7708", "openfda": {"unii": ["D1JT611TNE"], "spl_set_id": ["21b504bc-e12d-3a8e-e063-6294a90a7708"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-5031-41)", "package_ndc": "0220-5031-41", "marketing_start_date": "20240101"}], "brand_name": "Titanium metallicum", "product_id": "0220-5031_21b504bc-e12e-3a8e-e063-6294a90a7708", "dosage_form": "PELLET", "product_ndc": "0220-5031", "generic_name": "TITANIUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Titanium metallicum", "active_ingredients": [{"name": "TITANIUM", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}