Package 59883-030-04

Brand: fluoridex

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 59883-030-04
Digits Only 5988303004
Product NDC 59883-030
Product ID 59883-030_020d58ac-51bc-19a2-e063-6394a90aedf6
Description

1 TUBE in 1 BOX (59883-030-04) / 112 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2017-01-06
Brand fluoridex
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

FLUORIDEX ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "020d58ac-51bc-19a2-e063-6394a90aedf6", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["637365", "847014"], "spl_set_id": ["6050ef4d-50e8-55d7-e053-2991aa0ad076"], "manufacturer_name": ["DENT-MAT HOLDINGS, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (59883-030-04)  / 112 g in 1 TUBE", "package_ndc": "59883-030-04", "marketing_start_date": "20170106"}], "brand_name": "FLUORIDEX", "product_id": "59883-030_020d58ac-51bc-19a2-e063-6394a90aedf6", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "59883-030", "generic_name": "Sodium Fluoride", "labeler_name": "DENT-MAT HOLDINGS, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUORIDEX", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "5 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20170106", "listing_expiration_date": "20261231"}