NDC 69517-109

All Day Pain Relief

Naproxen Sodium Tablets, 220 Mg

All Day Pain Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Healthlife Of Usa Llc. The primary component is Naproxen Sodium.

• Product ID: 69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84b
• NDC: 69517-109
• Product Type: Human Otc Drug
• Proprietary Name: All Day Pain Relief
• Generic Name: Naproxen Sodium Tablets, 220 Mg
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2011-09-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA091353
• Labeler Name: HealthLife of USA LLC
• Substance Name: NAPROXEN SODIUM
• Active Ingredient Strength: 220 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69517-109-02

2 POUCH in 1 POUCH (69517-109-02) > 2 TABLET in 1 POUCH

• Marketing Start Date: 2016-04-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69517-109-02 [69517010902]

All Day Pain Relief TABLET

• Marketing Category: ANDA
• Application Number: ANDA091353
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-04-07

NDC 69517-109-25 [69517010925]

All Day Pain Relief TABLET

• Marketing Category: ANDA
• Application Number: ANDA091353
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-04-07

NDC 69517-109-01 [69517010901]

All Day Pain Relief TABLET

• Marketing Category: ANDA
• Application Number: ANDA091353
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-09-30

NDC 69517-109-24 [69517010924]

All Day Pain Relief TABLET

• Marketing Category: ANDA
• Application Number: ANDA091353
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-09-30

NDC 69517-109-50 [69517010950]

All Day Pain Relief TABLET

• Marketing Category: ANDA
• Application Number: ANDA091353
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-04-07

NDC 69517-109-04 [69517010904]

All Day Pain Relief TABLET

• Marketing Category: ANDA
• Application Number: ANDA091353
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-04-07

Drug Details

Active Ingredients

Ingredient	Strength
NAPROXEN SODIUM	220 mg/1

OpenFDA Data

• SPL SET ID: 7b0cb91e-5465-40ef-9f82-919f7d984f17
• Manufacturer:
  • HealthLife of USA LLC
• UNII:
  • 9TN87S3A3C
• RxNorm Concept Unique ID - RxCUI:
  • 849574
• UPC Code:
  • 0069517109248

NDC Crossover Matching brand name "All Day Pain Relief" or generic name "Naproxen Sodium Tablets, 220 Mg"

NDC	Brand Name	Generic Name
0363-0168	All Day Pain Relief	Naproxen Sodium
0363-0169	All Day Pain Relief	Naproxen Sodium
0363-0368	All Day Pain Relief	Naproxen Sodium
0363-0938	all day pain relief	Naproxen Sodium
0363-6099	ALL DAY PAIN RELIEF	NAPROXEN SODIUM
0363-9608	ALL DAY PAIN RELIEF	NAPROXEN SODIUM
15127-168	All Day Pain Relief	Naproxen Sodium
30142-168	All Day Pain Relief	Naproxen Sodium
33992-0169	All Day Pain Relief	Naproxen Sodium
36800-256	All Day Pain Relief	Naproxen Sodium
37205-744	All Day Pain Relief	Naproxen Sodium
37808-068	All Day Pain Relief	Naproxen Sodium
37808-259	All Day Pain Relief	Naproxen Sodium
37808-339	all day pain relief	Naproxen sodium
37808-500	All Day Pain Relief	Naproxen Sodium
41163-167	All Day Pain Relief	Naproxen Sodium
41163-169	All Day Pain Relief	Naproxen Sodium
42254-230	all day pain relief	Naproxen Sodium
49781-046	All Day Pain Relief	Naproxen Sodium
49781-047	All Day Pain Relief	Naproxen Sodium
49781-145	All Day Pain Relief	Naproxen Sodium
49781-146	All Day Pain Relief	Naproxen Sodium
68210-0030	ALL DAY PAIN RELIEF	ALL DAY PAIN RELIEF
69517-109	All Day Pain Relief	All Day Pain Relief
70005-008	All Day Pain Relief	All Day Pain Relief
49781-101	All Day Pain Relief	All Day Pain Relief
55315-168	All Day Pain Relief	All Day Pain Relief
55315-256	All Day Pain Relief	All Day Pain Relief
55315-255	All Day Pain Relief	All Day Pain Relief
55315-169	All Day Pain Relief	All Day Pain Relief
55319-417	All Day Pain Relief	All Day Pain Relief
55319-604	All Day Pain Relief	All Day Pain Relief
55319-174	All Day Pain Relief	All Day Pain Relief
59726-169	All Day Pain Relief	All Day Pain Relief
59779-172	All Day Pain Relief	All Day Pain Relief
59726-023	All Day Pain Relief	All Day Pain Relief
59726-168	All Day Pain Relief	All Day Pain Relief
59726-256	All Day Pain Relief	All Day Pain Relief
63940-174	All Day Pain Relief	All Day Pain Relief