ApprovalTrail

Ingredient

Naproxen Sodium

Products in Health Canada’s databases that list Naproxen Sodium as a medicinal or active ingredient. Its salts and forms that the databases name on their own have their own pages.

Drug products
44
27 authorized now
Natural health products
0
0 active licences
Notices of Compliance
88
Products in all
44

Drug products

Authorized products first.

NameDINStatus
ALEVE BACK AND BODY PAIN (220 MG)02436337Marketed
ALEVE CAPLETS (220 MG)02301733Marketed
ALEVE LIQUID GELS (220 MG)02361795Marketed
ALEVE NIGHTTIME (220 MG)02444593Marketed
ANAPROX (275 MG)02162725Marketed
ANAPROX DS (550 MG)02162717Marketed
APO-NAPRO-NA (275 MG)00784354Marketed
APO-NAPRO-NA DS (550 MG)01940309Marketed
JAMP SUMATRIPTAN / NAPROXEN SODIUM (500 MG)02566974Marketed
MAXIDOL LIQUID GELS (220 MG)02372991Marketed
NAPROXEN (220 MG)02362430Marketed
NAPROXEN MENSTRUAL PAIN RELIEF (220 MG)02396009Marketed
NAPROXEN-NA (275 MG)00887056Marketed
NAPROXEN-NA DF (550 MG)02153386Marketed
SUVEXX (500 MG)02496305Marketed
TEVA-NAPROXEN SODIUM (275 MG)00778389Marketed
TEVA-NAPROXEN SODIUM DS (550 MG)02026600Marketed
APO-SUMATRIPTAN-NAPROXEN SODIUM (500 MG)02570165Approved
NAPROXEN LIQUID GELS (220 MG)02442922Approved
NAPROXEN SODIUM CAPLETS (220 MG)02379309Approved
NAPROXEN SODIUM CAPSULES (220 MG)02475227Approved
NAPROXEN SODIUM TABLETS (220 MG)02378876Approved
NAPROXEN SODIUM TABLETS (220 MG)02385007Dormant
NAPROXEN SODIUM TABLETS USP 220 MG (220 MG)02561581Approved
PAIN RELIEVER & SLEEP AID (220 MG)02506378Approved
WAYMADE-NAPROXEN SODIUM (275 MG)02463695Approved
WAYMADE-NAPROXEN SODIUM DS (550 MG)02463709Approved
ANAPROX (275 MG)00491772Cancelled Post Market
ANAPROX DS TAB 550MG (550 MG)00869031Cancelled Post Market
MOTRIMAX 12 HOUR TABLETS (220 MG)02423790Cancelled Pre Market
NAPROXEN (220 MG)02378418Cancelled Post Market
NAPROXEN (220 MG)02408759Cancelled Post Market
NAPROXEN CAPSULES 200 MG (105 MG)02422743Cancelled Pre Market
NAPROXEN SODIUM (275 MG)02351013Cancelled Post Market
NAPROXEN SODIUM DS (550 MG)02351021Cancelled Post Market
NTP-NAPROXEN SODIUM (275 MG)02347334Cancelled Pre Market
NTP-NAPROXEN SODIUM DS (550 MG)02347369Cancelled Pre Market
NU-NAPRO-NA (275 MG)02336596Cancelled (Unreturned Annual)
NU-NAPRO-NA DS (550 MG)02336618Cancelled (Unreturned Annual)
NX 12 HOUR (220 MG)02378663Cancelled Pre Market
RIVA-NAPROXEN SODIUM (275 MG)02240827Cancelled Post Market
RIVA-NAPROXEN SODIUM DS (550 MG)02240828Cancelled Post Market
SYNFLEX DS TAB 550MG (550 MG)01900897Cancelled Post Market
SYNFLEX TAB 275MG (275 MG)00675369Cancelled Post Market

Notices of Compliance

Approvals of drug submissions that list it, newest first.