Package 59883-020-04

Brand: fluoridex

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 59883-020-04
Digits Only 5988302004
Product NDC 59883-020
Product ID 59883-020_82f8eacb-a214-3080-e053-2a91aa0a6a07
Description

1 TUBE in 1 BOX (59883-020-04) / 112 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2017-01-03
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": "82f8eacb-a214-3080-e053-2a91aa0a6a07", "openfda": {"unii": ["8ZYQ1474W7"], "spl_set_id": ["6014c330-3698-027c-e053-2a91aa0a64e5"], "manufacturer_name": ["DEN-MAT HOLDINGS, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (59883-020-04)  / 112 g in 1 TUBE", "package_ndc": "59883-020-04", "marketing_start_date": "20170103"}], "brand_name": "FLUORIDEX", "product_id": "59883-020_82f8eacb-a214-3080-e053-2a91aa0a6a07", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "59883-020", "generic_name": "Sodium Fluoride", "labeler_name": "DEN-MAT HOLDINGS, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUORIDEX", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "5 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20170103", "listing_expiration_date": "20261231"}