NUPRO TOPICAL SODIUM FLUORIDE NEUTRAL - GEL

Approval Id: 031f273db491b0a8
Drug Approval Canada Name: NUPRO TOPICAL SODIUM FLUORIDE NEUTRAL - GEL
Product Name: NUPRO TOPICAL SODIUM FLUORIDE NEUTRAL - GEL
Status: Cancelled Post Market
Status Date: 2008-06-20
Original Market Date: 1995-12-31
Din: 02015250
Drug Class: Human
Dosage Form: Gel
Route Of Administration: Topical
Schedule: OTC
Ahfs: 34:00.00
Atc Original: A01AA01 SODIUM FLUORIDE
Atc Name: a 01 aa 01
Aig Number: 0107147009
Company Name: DENTSPLY INTERNATIONAL
Company Address: 60, 221 West Philadelphia Street, York, Pennsylvania, United States, 17401
Company Detail Path: /organization/dentsply-international

SODIUM FLUORIDE

2 %

Authorized

Agency

Health Canada

Country

🇨🇦

Approval Date

Jul 4, 2025

Approval ID

031f273db491b0a8

Type

Standard