Package 42291-741-51

Brand: sodium flouride

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 42291-741-51
Digits Only 4229174151
Product NDC 42291-741
Description

1 TUBE in 1 CARTON (42291-741-51) / 53.2 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2019-09-20
Brand sodium flouride
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "4874ee42-bfbe-02d5-e063-6394a90a2b6e", "openfda": {"upc": ["0342291741515"], "unii": ["8ZYQ1474W7"], "spl_set_id": ["92fef2e0-f9f2-8b0f-e053-2995a90a096a"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (42291-741-51)  / 53.2 mL in 1 TUBE", "package_ndc": "42291-741-51", "marketing_start_date": "20190920"}], "brand_name": "Sodium Flouride", "product_id": "42291-741_4874ee42-bfbe-02d5-e063-6394a90a2b6e", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "42291-741", "generic_name": "Sodium Fluoride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Flouride", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "5 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20190920", "listing_expiration_date": "20271231"}