Package 69367-312-01

Brand: sodium fluoride 5000 ppm

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 69367-312-01
Digits Only 6936731201
Product NDC 69367-312
Description

100 mL in 1 TUBE (69367-312-01)

Marketing

Marketing Status
Marketed Since 2021-06-16
Brand sodium fluoride 5000 ppm
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "f227132c-6257-4245-b8e0-7de78c15c201", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["392038"], "spl_set_id": ["56efb346-c715-463d-9260-f7fcfbd2b70f"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 TUBE (69367-312-01)", "package_ndc": "69367-312-01", "marketing_start_date": "20210616"}], "brand_name": "Sodium Fluoride 5000 PPM", "product_id": "69367-312_f227132c-6257-4245-b8e0-7de78c15c201", "dosage_form": "PASTE", "product_ndc": "69367-312", "generic_name": "Sodium Fluoride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride 5000 PPM", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "6 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210616", "listing_expiration_date": "20261231"}