Package 0220-0632-41

Brand: aurum iodatum

Generic: gold monoiodide
NDC Package

Package Facts

Identity

Package NDC 0220-0632-41
Digits Only 0220063241
Product NDC 0220-0632
Description

6 [hp_C] in 1 TUBE (0220-0632-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand aurum iodatum
Generic gold monoiodide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bf73fbe-fa38-c3d8-e063-6294a90aef07", "openfda": {"unii": ["T1UDV7ES1A"], "spl_set_id": ["6c40ea02-4076-3880-e053-2991aa0ad6c1"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-0632-41)", "package_ndc": "0220-0632-41", "marketing_start_date": "19830303"}], "brand_name": "Aurum iodatum", "product_id": "0220-0632_3bf73fbe-fa38-c3d8-e063-6294a90aef07", "dosage_form": "PELLET", "product_ndc": "0220-0632", "generic_name": "GOLD MONOIODIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aurum iodatum", "active_ingredients": [{"name": "GOLD MONOIODIDE", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}