NDC 69621-365

Lexixryl

Diclofenac Sodium

Lexixryl is a Kit in the Human Prescription Drug category. It is labeled and distributed by Shoreline Pharmaceuticals, Inc.. The primary component is .

Product ID69621-365_054ab420-32ab-4237-b640-abada8896e9c
NDC69621-365
Product TypeHuman Prescription Drug
Proprietary NameLexixryl
Generic NameDiclofenac Sodium
Dosage FormKit
Marketing Start Date2016-11-08
Marketing CategoryANDA / ANDA
Application NumberANDA202769
Labeler NameShoreline Pharmaceuticals, Inc.
Active Ingredient Strength0
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 69621-365-00

1 KIT in 1 PACKAGE (69621-365-00) * 1 BOTTLE in 1 CARTON (59088-372-10) > 150 mL in 1 BOTTLE * 30 in 1 CARTON
Marketing Start Date2016-11-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69621-365-00 [69621036500]

Lexixryl KIT
Marketing CategoryANDA
Application NumberANDA202769
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-11-08
Marketing End Date2019-05-16

Drug Details

OpenFDA Data

SPL SET ID:3e80fb62-480a-4930-ae87-bb85c6c35a2a
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 857700
  • NDC Crossover Matching brand name "Lexixryl" or generic name "Diclofenac Sodium"

    NDCBrand NameGeneric Name
    69621-365LexixrylLexixryl
    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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