Package 48951-3280-2

Brand: cuprum 0.4

Generic: cuprum 0.4
NDC Package

Package Facts

Identity

Package NDC 48951-3280-2
Digits Only 4895132802
Product NDC 48951-3280
Product ID 48951-3280_2c8fc7ec-a8ff-7468-e063-6294a90ae355
Description

30 g in 1 TUBE (48951-3280-2)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand cuprum 0.4
Generic cuprum 0.4
Sample Package No

Linked Drug Pages (1)

Cuprum 0.4 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2c8fc7ec-a8ff-7468-e063-6294a90ae355", "openfda": {"nui": ["M0005152", "N0000175831", "N0000008595", "N0000008924", "N0000175830"], "unii": ["789U1901C5"], "spl_set_id": ["2c8fc7ec-a8fe-7468-e063-6294a90ae355"], "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": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 TUBE (48951-3280-2)", "package_ndc": "48951-3280-2", "marketing_start_date": "20090901"}], "brand_name": "Cuprum 0.4", "product_id": "48951-3280_2c8fc7ec-a8ff-7468-e063-6294a90ae355", "dosage_form": "OINTMENT", "pharm_class": ["Copper [CS]", "Copper-containing Intrauterine Device [EPC]", "Decreased Embryonic Implantation [PE]", "Decreased Sperm Motility [PE]", "Inhibit Ovum Fertilization [PE]"], "product_ndc": "48951-3280", "generic_name": "Cuprum 0.4", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cuprum 0.4", "active_ingredients": [{"name": "COPPER", "strength": "1 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}