Package 61480-127-05

Brand: eczemol

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

Package Facts

Identity

Package NDC 61480-127-05
Digits Only 6148012705
Product NDC 61480-127
Description

100 TABLET in 1 BOTTLE (61480-127-05)

Marketing

Marketing Status
Marketed Since 2001-11-15
Brand eczemol
Generic potassium bromide, nickel sulfate, and sulfur
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "440c8a06-8ffb-f7af-e063-6394a90a7ccf", "openfda": {"upc": ["0361480127053"], "unii": ["4FLT4T3WUN", "OSD78555ZM", "70FD1KFU70"], "spl_set_id": ["981e9f3d-b608-4a5e-92f8-895b22da12f4"], "manufacturer_name": ["PLYMOUTH HEALTHCARE PRODUCTS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (61480-127-05)", "package_ndc": "61480-127-05", "marketing_start_date": "20011115"}], "brand_name": "Eczemol", "product_id": "61480-127_440c8a06-8ffb-f7af-e063-6394a90a7ccf", "dosage_form": "TABLET", "product_ndc": "61480-127", "generic_name": "Potassium Bromide, Nickel Sulfate, and Sulfur", "labeler_name": "PLYMOUTH HEALTHCARE PRODUCTS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eczemol", "active_ingredients": [{"name": "NICKEL SULFATE", "strength": "1 [hp_X]/1"}, {"name": "POTASSIUM BROMIDE", "strength": "1 [hp_X]/1"}, {"name": "SULFUR", "strength": "1 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20011115", "listing_expiration_date": "20261231"}