NDC 56062-878

arthritis pain reliever

Diclofenac Sodium

arthritis pain reliever is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Publix Super Markets Inc. The primary component is Diclofenac Sodium.

Product ID56062-878_0d062516-fe38-4862-bed8-41f5acc3a7b6
Product TypeHuman Otc Drug
Proprietary Namearthritis pain reliever
Generic NameDiclofenac Sodium
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2021-02-01
Marketing CategoryANDA /
Application NumberANDA211253
Labeler NamePublix Super Markets Inc
Active Ingredient Strength10 mg/g
NDC Exclude FlagN
Listing Certified Through2022-12-31


NDC 56062-878-02

1 TUBE in 1 CARTON (56062-878-02) > 50 g in 1 TUBE
Marketing Start Date2021-02-01
NDC Exclude FlagN
Sample Package?N

Drug Details

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

NDCBrand NameGeneric Name
0363-0544arthritis pain relieverAcetaminophen
0363-9781Arthritis Pain RelieverAcetaminophen
68071-1552Arthritis Pain RelieverArthritis Pain Reliever
68084-777Arthritis Pain RelieverArthritis Pain Reliever
33261-665Arthritis Pain RelieverArthritis Pain Reliever
50268-052Arthritis Pain RelieverArthritis Pain Reliever
51660-333Arthritis Pain RelieverArthritis Pain Reliever
55700-679Arthritis Pain RelieverArthritis Pain Reliever
59092-001Arthritis Pain RelieverArthritis Pain Reliever
66336-233Arthritis Pain RelieverArthritis 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
0113-1189good sense arthritis paindiclofenac sodium
0067-8152Voltarendiclofenac sodium
0067-8153Voltarendiclofenac sodium
0078-0478VOLTARENdiclofenac sodium

© 2023 FDA.report
This site is not affiliated with or endorsed by the FDA.