Package 0220-0648-41
Brand: aurum muriaticum natronatum
Generic: sodium tetrachloroauratePackage Facts
Identity
Package NDC
0220-0648-41
Digits Only
0220064841
Product NDC
0220-0648
Description
4 [hp_C] in 1 TUBE (0220-0648-41)
Marketing
Marketing Status
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": "09acb03c-1113-b167-e063-6394a90aaee1", "openfda": {"unii": ["7FT6QUT299"], "spl_set_id": ["84005c8d-3ff5-48bb-e053-2a91aa0ab3b4"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 [hp_C] in 1 TUBE (0220-0648-41)", "package_ndc": "0220-0648-41", "marketing_start_date": "19830303"}], "brand_name": "Aurum muriaticum natronatum", "product_id": "0220-0648_09acb03c-1113-b167-e063-6394a90aaee1", "dosage_form": "PELLET", "product_ndc": "0220-0648", "generic_name": "SODIUM TETRACHLOROAURATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aurum muriaticum natronatum", "active_ingredients": [{"name": "SODIUM TETRACHLOROAURATE", "strength": "4 [hp_C]/4[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}