NDC 0067-8153

Voltaren Arthritis Pain

Diclofenac Sodium

Voltaren Arthritis Pain is a Kit in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is .

• Product ID: 0067-8153_051c7983-b0ec-4d0b-8212-66415f6e3058
• NDC: 0067-8153
• Product Type: Human Otc Drug
• Proprietary Name: Voltaren Arthritis Pain
• Generic Name: Diclofenac Sodium
• Dosage Form: Kit
• Marketing Start Date: 2020-05-13
• Marketing Category: NDA / NDA
• Application Number: NDA022122
• Labeler Name: GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0067-8153-01

1 KIT in 1 CARTON (0067-8153-01) * 2 TUBE in 1 KIT > 150 g in 1 TUBE * 1 TUBE in 1 KIT > 50 g in 1 TUBE

• Marketing Start Date: 2020-05-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0067-8153-01 [00067815301]

Voltaren Arthritis Pain KIT

• Marketing Category: NDA
• Application Number: NDA022122
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-05-13

Drug Details

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

NDC	Brand Name	Generic Name
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