Package 0220-1620-41
Brand: cuprum oxydatum nigrum
Generic: cupric oxidePackage Facts
Identity
Package NDC
0220-1620-41
Digits Only
0220162041
Product NDC
0220-1620
Description
200 [kp_C] in 1 TUBE (0220-1620-41)
Marketing
Marketing Status
Brand
cuprum oxydatum nigrum
Generic
cupric oxide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "163cb0dd-0f64-4e32-e063-6394a90a4608", "openfda": {"unii": ["V1XJQ704R4"], "spl_set_id": ["163cb0dd-0f63-4e32-e063-6394a90a4608"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-1620-41)", "package_ndc": "0220-1620-41", "marketing_start_date": "20240101"}], "brand_name": "Cuprum oxydatum nigrum", "product_id": "0220-1620_163cb0dd-0f64-4e32-e063-6394a90a4608", "dosage_form": "PELLET", "product_ndc": "0220-1620", "generic_name": "CUPRIC OXIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cuprum oxydatum nigrum", "active_ingredients": [{"name": "CUPRIC OXIDE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}