Package 0220-1648-41

Brand: cuprum metallicum

Generic: copper
NDC Package

Package Facts

Identity

Package NDC 0220-1648-41
Digits Only 0220164841
Product NDC 0220-1648
Description

1 [hp_M] in 1 TUBE (0220-1648-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "0a0c91f9-28af-3d6d-e063-6294a90aec12", "openfda": {"nui": ["M0005152", "N0000175831", "N0000008595", "N0000008924", "N0000175830"], "unii": ["789U1901C5"], "spl_set_id": ["857a1e8d-20df-44a0-e053-2991aa0abb22"], "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": "1 [hp_M] in 1 TUBE (0220-1648-41)", "package_ndc": "0220-1648-41", "marketing_start_date": "19830303"}], "brand_name": "Cuprum metallicum", "product_id": "0220-1648_0a0c91f9-28af-3d6d-e063-6294a90aec12", "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": "0220-1648", "generic_name": "COPPER", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cuprum metallicum", "active_ingredients": [{"name": "COPPER", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}