Package 69367-309-51

Brand: sodium fluoride 5000 plus

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 69367-309-51
Digits Only 6936730951
Product NDC 69367-309
Product ID 69367-309_2c5374da-64f6-41f0-8b2a-f23c76dbc3a5
Description

1 TUBE in 1 CARTON (69367-309-51) / 51 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-03-09
Brand sodium fluoride 5000 plus
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

Sodium Fluoride 5000 Plus ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "2c5374da-64f6-41f0-8b2a-f23c76dbc3a5", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["392038"], "spl_set_id": ["157b975e-0229-4081-8d7d-b5f933e178e0"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69367-309-51)  / 51 g in 1 TUBE", "package_ndc": "69367-309-51", "marketing_start_date": "20210309"}], "brand_name": "Sodium Fluoride 5000 Plus", "product_id": "69367-309_2c5374da-64f6-41f0-8b2a-f23c76dbc3a5", "dosage_form": "CREAM", "product_ndc": "69367-309", "generic_name": "Sodium Fluoride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride 5000 Plus", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "5 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210309", "listing_expiration_date": "20261231"}