Package 0220-0649-41

Brand: aurum muriaticum natronatum

Generic: sodium tetrachloroaurate
NDC Package

Package Facts

Identity

Package NDC 0220-0649-41
Digits Only 0220064941
Product NDC 0220-0649
Description

9 [hp_C] in 1 TUBE (0220-0649-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand aurum muriaticum natronatum
Generic sodium tetrachloroaurate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09acadb7-c0a1-d753-e063-6294a90af9a9", "openfda": {"unii": ["7FT6QUT299"], "spl_set_id": ["84005bc3-6562-5b9d-e053-2991aa0aef14"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-0649-41)", "package_ndc": "0220-0649-41", "marketing_start_date": "19830303"}], "brand_name": "Aurum muriaticum natronatum", "product_id": "0220-0649_09acadb7-c0a1-d753-e063-6294a90af9a9", "dosage_form": "PELLET", "product_ndc": "0220-0649", "generic_name": "SODIUM TETRACHLOROAURATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aurum muriaticum natronatum", "active_ingredients": [{"name": "SODIUM TETRACHLOROAURATE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}