Package 48951-3124-5

Brand: copper oxide 0.4

Generic: copper oxide 0.4
NDC Package

Package Facts

Identity

Package NDC 48951-3124-5
Digits Only 4895131245
Product NDC 48951-3124
Description

60 g in 1 TUBE (48951-3124-5)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "389362be-d335-f00c-e063-6294a90a61b6", "openfda": {"unii": ["V1XJQ704R4"], "spl_set_id": ["3987be95-ba66-4f2e-9255-351d799ac304"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 TUBE (48951-3124-5)", "package_ndc": "48951-3124-5", "marketing_start_date": "20090901"}], "brand_name": "Copper Oxide 0.4", "product_id": "48951-3124_389362be-d335-f00c-e063-6294a90a61b6", "dosage_form": "OINTMENT", "product_ndc": "48951-3124", "generic_name": "Copper Oxide 0.4", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Copper Oxide 0.4", "active_ingredients": [{"name": "CUPRIC OXIDE", "strength": "1 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}