Package 0220-0856-41

Brand: bismuthum metallicum

Generic: bismuth
NDC Package

Package Facts

Identity

Package NDC 0220-0856-41
Digits Only 0220085641
Product NDC 0220-0856
Description

200 [kp_C] in 1 TUBE (0220-0856-41)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1639b073-f5ce-ddb2-e063-6294a90a4419", "openfda": {"unii": ["U015TT5I8H"], "spl_set_id": ["1639b073-f5cd-ddb2-e063-6294a90a4419"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0856-41)", "package_ndc": "0220-0856-41", "marketing_start_date": "20240101"}], "brand_name": "Bismuthum metallicum", "product_id": "0220-0856_1639b073-f5ce-ddb2-e063-6294a90a4419", "dosage_form": "PELLET", "product_ndc": "0220-0856", "generic_name": "BISMUTH", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bismuthum metallicum", "active_ingredients": [{"name": "BISMUTH", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}