Package 61480-124-05

Brand: psorizide ultra

Generic: potassium bromide, nickel sulfate, and zinc bromide
NDC Package

Package Facts

Identity

Package NDC 61480-124-05
Digits Only 6148012405
Product NDC 61480-124
Description

100 TABLET in 1 BOTTLE (61480-124-05)

Marketing

Marketing Status
Marketed Since 1997-10-01
Brand psorizide ultra
Generic potassium bromide, nickel sulfate, and zinc bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b242c2f-68f0-089a-e063-6394a90a405f", "openfda": {"upc": ["0361480124052"], "unii": ["4FLT4T3WUN", "OSD78555ZM", "OO7ZBU9703"], "spl_set_id": ["78d05c25-6817-4763-b662-6dbb0625fa84"], "manufacturer_name": ["PLYMOUTH HEALTHCARE PRODUCTS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (61480-124-05)", "package_ndc": "61480-124-05", "marketing_start_date": "19971001"}], "brand_name": "Psorizide Ultra", "product_id": "61480-124_2b242c2f-68f0-089a-e063-6394a90a405f", "dosage_form": "TABLET", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "61480-124", "generic_name": "Potassium Bromide, Nickel Sulfate, and Zinc Bromide", "labeler_name": "PLYMOUTH HEALTHCARE PRODUCTS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Psorizide Ultra", "active_ingredients": [{"name": "NICKEL SULFATE", "strength": "1 [hp_X]/1"}, {"name": "POTASSIUM BROMIDE", "strength": "1 [hp_X]/1"}, {"name": "ZINC BROMIDE", "strength": "4 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19971001", "listing_expiration_date": "20261231"}