Package 0220-0644-41

Brand: aurum muriaticum kalinatum

Generic: potassium tetrachloroaurate dihydrate
NDC Package

Package Facts

Identity

Package NDC 0220-0644-41
Digits Only 0220064441
Product NDC 0220-0644
Product ID 0220-0644_09ac80f8-325d-a443-e063-6394a90a1438
Description

9 [hp_C] in 1 TUBE (0220-0644-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand aurum muriaticum kalinatum
Generic potassium tetrachloroaurate dihydrate
Sample Package No

Linked Drug Pages (1)

Aurum muriaticum kalinatum ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "09ac80f8-325d-a443-e063-6394a90a1438", "openfda": {"unii": ["SYJ0T39LVU"], "spl_set_id": ["84749c71-5f3c-2dda-e053-2991aa0aed8d"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-0644-41)", "package_ndc": "0220-0644-41", "marketing_start_date": "19830303"}], "brand_name": "Aurum muriaticum kalinatum", "product_id": "0220-0644_09ac80f8-325d-a443-e063-6394a90a1438", "dosage_form": "PELLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0220-0644", "generic_name": "POTASSIUM TETRACHLOROAURATE DIHYDRATE", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aurum muriaticum kalinatum", "active_ingredients": [{"name": "POTASSIUM TETRACHLOROAURATE DIHYDRATE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}