Package 63783-504-06

Brand: neutra maxx 5000

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 63783-504-06
Digits Only 6378350406
Product NDC 63783-504
Product ID 63783-504_cb8064d7-2d0f-4860-b794-d90a121761ad
Description

120 g in 1 BOTTLE, DISPENSING (63783-504-06)

Marketing

Marketing Status
Marketed Since 1989-01-01
Brand neutra maxx 5000
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

NEUTRA MAXX 5000 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cb8064d7-2d0f-4860-b794-d90a121761ad", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["392038", "1191716"], "spl_set_id": ["fcbe6baa-2827-49df-9316-42cc86595203"], "manufacturer_name": ["Massco Dental A Division of Dunagin Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 g in 1 BOTTLE, DISPENSING (63783-504-06)", "package_ndc": "63783-504-06", "marketing_start_date": "19890101"}], "brand_name": "NEUTRA MAXX 5000", "product_id": "63783-504_cb8064d7-2d0f-4860-b794-d90a121761ad", "dosage_form": "GEL", "product_ndc": "63783-504", "generic_name": "SODIUM FLUORIDE", "labeler_name": "Massco Dental A Division of Dunagin Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEUTRA MAXX 5000", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "1.428 g/120g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19890101", "listing_expiration_date": "20261231"}