NDC 59088-365

Xrylix

Diclofenac Sodium

Xrylix is a Kit in the Human Prescription Drug category. It is labeled and distributed by Puretek Corporation. The primary component is .

• Product ID: 59088-365_1cf91296-f475-4373-bb0d-3fb7eabe6308
• NDC: 59088-365
• Product Type: Human Prescription Drug
• Proprietary Name: Xrylix
• Generic Name: Diclofenac Sodium
• Dosage Form: Kit
• Marketing Start Date: 2016-03-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA202769
• Labeler Name: PureTek Corporation
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 59088-365-00

1 KIT in 1 PACKAGE (59088-365-00) * 1 BOTTLE in 1 CARTON (59088-372-10) > 150 mL in 1 BOTTLE

• Marketing Start Date: 2017-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59088-365-00 [59088036500]

Xrylix KIT

• Marketing Category: ANDA
• Application Number: ANDA202769
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-03-01

Drug Details

OpenFDA Data

• SPL SET ID: f8f10213-b92c-45ba-adf6-ebb2f91ca1a8
• Manufacturer:
  • PureTek Corporation
• RxNorm Concept Unique ID - RxCUI:
  • 857700

NDC Crossover Matching brand name "Xrylix" or generic name "Diclofenac Sodium"

NDC	Brand Name	Generic Name
59088-365	Xrylix	Xrylix
0280-0039	Aleve Arthritis Pain Gel	Diclofenac Sodium
0115-1483	Diclofenac Sodium	Diclofenac Sodium
0168-0803	DICLOFENAC SODIUM	diclofenac sodium
0168-0844	DICLOFENAC SODIUM	diclofenac sodium
0228-2550	Diclofenac Sodium	Diclofenac Sodium
0228-2551	Diclofenac Sodium	Diclofenac Sodium
0363-1210	Diclofenac sodium	Diclofenac sodium
0363-1871	diclofenac sodium	diclofenac sodium
0378-0355	Diclofenac Sodium	Diclofenac Sodium
0378-6280	Diclofenac Sodium	diclofenac sodium
0378-6281	Diclofenac Sodium	diclofenac sodium
0113-1189	good sense arthritis pain	diclofenac sodium
0067-8152	Voltaren	diclofenac sodium
0067-8153	Voltaren	diclofenac sodium
0078-0478	VOLTAREN	diclofenac sodium