NDC 70677-0108

Sunmark Arthritis Pain

Diclofenac Sodium

Sunmark Arthritis Pain is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Strategic Sourcing Services Llc. The primary component is Diclofenac Sodium.

Product ID70677-0108_2a0c3d70-6193-4603-a046-0f7a74fc2076
NDC70677-0108
Product TypeHuman Otc Drug
Proprietary NameSunmark Arthritis Pain
Generic NameDiclofenac Sodium
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-06-03
Marketing CategoryANDA / ANDA
Application NumberANDA211253
Labeler NameStrategic Sourcing Services LLC
Substance NameDICLOFENAC SODIUM
Active Ingredient Strength10 mg/g
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 70677-0108-1

1 TUBE in 1 CARTON (70677-0108-1) > 100 g in 1 TUBE
Marketing Start Date2020-06-03
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Sunmark Arthritis Pain" or generic name "Diclofenac Sodium"

NDCBrand NameGeneric Name
70677-0108Sunmark Arthritis PainSunmark Arthritis Pain
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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