Package 0220-0859-41

Brand: bismuthum subnitricum

Generic: bismuth subnitrate
NDC Package

Package Facts

Identity

Package NDC 0220-0859-41
Digits Only 0220085941
Product NDC 0220-0859
Product ID 0220-0859_07d93bfb-dc2d-65aa-e063-6394a90a3761
Description

30 [hp_C] in 1 TUBE (0220-0859-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "07d93bfb-dc2d-65aa-e063-6394a90a3761", "openfda": {"unii": ["H19J064BA5"], "spl_set_id": ["840e9b46-28c5-35d2-e053-2991aa0a4968"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0859-41)", "package_ndc": "0220-0859-41", "marketing_start_date": "19830303"}], "brand_name": "Bismuthum subnitricum", "product_id": "0220-0859_07d93bfb-dc2d-65aa-e063-6394a90a3761", "dosage_form": "PELLET", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "0220-0859", "generic_name": "BISMUTH SUBNITRATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bismuthum subnitricum", "active_ingredients": [{"name": "BISMUTH SUBNITRATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}