Package 0220-1636-41
Brand: cuprum metallicum
Generic: copperPackage Facts
Identity
Package NDC
0220-1636-41
Digits Only
0220163641
Product NDC
0220-1636
Description
200 [kp_C] in 1 TUBE (0220-1636-41)
Marketing
Marketing Status
Brand
cuprum metallicum
Generic
copper
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f228fd4a-e34c-56df-e053-2a95a90a65d6", "openfda": {"nui": ["M0005152", "N0000175831", "N0000008595", "N0000008924", "N0000175830"], "unii": ["789U1901C5"], "spl_set_id": ["857a0e2a-2731-467f-e053-2991aa0a8cc6"], "pharm_class_cs": ["Copper [CS]"], "pharm_class_pe": ["Decreased Embryonic Implantation [PE]", "Decreased Sperm Motility [PE]", "Inhibit Ovum Fertilization [PE]"], "pharm_class_epc": ["Copper-containing Intrauterine Device [EPC]"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-1636-41)", "package_ndc": "0220-1636-41", "marketing_start_date": "19830303"}], "brand_name": "Cuprum metallicum", "product_id": "0220-1636_f228fd4a-e34c-56df-e053-2a95a90a65d6", "dosage_form": "PELLET", "pharm_class": ["Copper [CS]", "Copper-containing Intrauterine Device [EPC]", "Decreased Embryonic Implantation [PE]", "Decreased Sperm Motility [PE]", "Inhibit Ovum Fertilization [PE]"], "product_ndc": "0220-1636", "generic_name": "COPPER", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cuprum metallicum", "active_ingredients": [{"name": "COPPER", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}