Package 0220-0860-41

Brand: bismuthum subnitricum

Generic: bismuth subnitrate
NDC Package

Package Facts

Identity

Package NDC 0220-0860-41
Digits Only 0220086041
Product NDC 0220-0860
Product ID 0220-0860_39e8a434-0720-b2b0-e063-6294a90acd00
Description

200 [kp_C] in 1 TUBE (0220-0860-41)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand bismuthum subnitricum
Generic bismuth subnitrate
Sample Package No

Linked Drug Pages (1)

BISMUTHUM SUBNITRICUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39e8a434-0720-b2b0-e063-6294a90acd00", "openfda": {"unii": ["H19J064BA5"], "spl_set_id": ["39e8a434-071f-b2b0-e063-6294a90acd00"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0860-41)", "package_ndc": "0220-0860-41", "marketing_start_date": "20250101"}], "brand_name": "BISMUTHUM SUBNITRICUM", "product_id": "0220-0860_39e8a434-0720-b2b0-e063-6294a90acd00", "dosage_form": "PELLET", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "0220-0860", "generic_name": "BISMUTH SUBNITRATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BISMUTHUM SUBNITRICUM", "active_ingredients": [{"name": "BISMUTH SUBNITRATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}