NDC 11673-569

up and up arthritis pain reliever

Diclofenac Sodium

up and up arthritis pain reliever is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Diclofenac Sodium.

Product ID11673-569_0c61f8c4-3483-4202-bdd2-61721df6912b
NDC11673-569
Product TypeHuman Otc Drug
Proprietary Nameup and up arthritis pain reliever
Generic NameDiclofenac Sodium
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-08-19
Marketing CategoryANDA / ANDA
Application NumberANDA211253
Labeler NameTarget Corporation
Substance NameDICLOFENAC SODIUM
Active Ingredient Strength10 mg/g
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 11673-569-01

1 TUBE in 1 CARTON (11673-569-01) > 100 g in 1 TUBE
Marketing Start Date2020-08-19
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "up and up arthritis pain reliever" or generic name "Diclofenac Sodium"

NDCBrand NameGeneric Name
11673-569up and up arthritis pain relieverup and up arthritis pain reliever
0280-0039Aleve Arthritis Pain GelDiclofenac Sodium
0115-1483Diclofenac SodiumDiclofenac Sodium
0168-0803DICLOFENAC SODIUMdiclofenac sodium
0168-0844DICLOFENAC SODIUMdiclofenac sodium
0228-2550Diclofenac SodiumDiclofenac Sodium
0228-2551Diclofenac SodiumDiclofenac Sodium
0363-1210Diclofenac sodiumDiclofenac sodium
0363-1871diclofenac sodiumdiclofenac sodium
0378-0355Diclofenac SodiumDiclofenac Sodium
0378-6280Diclofenac Sodiumdiclofenac sodium
0378-6281Diclofenac Sodiumdiclofenac sodium
0113-1189good sense arthritis paindiclofenac sodium
0067-8152Voltarendiclofenac sodium
0067-8153Voltarendiclofenac sodium
0078-0478VOLTARENdiclofenac sodium
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