Package 55346-0943-1

Brand: alpha-pro

Generic: sodium fluoride and hydrofluoric acid
NDC Package

Package Facts

Identity

Package NDC 55346-0943-1
Digits Only 5534609431
Product NDC 55346-0943
Product ID 55346-0943_42c899b3-99ed-0863-e063-6394a90ad112
Description

497 g in 1 BOTTLE (55346-0943-1)

Marketing

Marketing Status
Marketed Since 2013-04-01
Brand alpha-pro
Generic sodium fluoride and hydrofluoric acid
Sample Package No

Linked Drug Pages (1)

Alpha-Pro ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "42c899b3-99ed-0863-e063-6394a90ad112", "openfda": {"unii": ["RGL5YE86CZ", "8ZYQ1474W7"], "rxcui": ["1297381"], "spl_set_id": ["a86ec65f-f6e1-474d-aeff-412a4716a92c"], "manufacturer_name": ["Dental Technologies, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "497 g in 1 BOTTLE (55346-0943-1)", "package_ndc": "55346-0943-1", "marketing_start_date": "20130401"}], "brand_name": "Alpha-Pro", "product_id": "55346-0943_42c899b3-99ed-0863-e063-6394a90ad112", "dosage_form": "GEL", "product_ndc": "55346-0943", "generic_name": "Sodium Fluoride and Hydrofluoric Acid", "labeler_name": "Dental Technologies, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alpha-Pro", "active_ingredients": [{"name": "HYDROFLUORIC ACID", "strength": "4.4 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "7.9 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20130401", "listing_expiration_date": "20261231"}