NDC 53185-362

Naproxen Sodium 220mg

Naproxen Sodium 220mg

Naproxen Sodium 220mg is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Athlete's Needs, Inc.. The primary component is Naproxen Sodium.

• Product ID: 53185-362_0fd72767-4371-4130-958d-4fdf4b05ead7
• NDC: 53185-362
• Product Type: Human Otc Drug
• Proprietary Name: Naproxen Sodium 220mg
• Generic Name: Naproxen Sodium 220mg
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2014-12-23
• Marketing Category: ANDA / ANDA
• Application Number: ANDA090545
• Labeler Name: Athlete's Needs, Inc.
• Substance Name: NAPROXEN SODIUM
• Active Ingredient Strength: 220 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 53185-362-50

50 TABLET, COATED in 1 BOTTLE (53185-362-50)

• Marketing Start Date: 2014-12-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 53185-362-50 [53185036250]

Naproxen Sodium 220mg TABLET, COATED

• Marketing Category: ANDA
• Application Number: ANDA090545
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-12-23

Drug Details

Active Ingredients

Ingredient	Strength
NAPROXEN SODIUM	220 mg/1

OpenFDA Data

• SPL SET ID: 91e1fef2-0e9b-4553-92f2-ddf219990695
• Manufacturer:
  • Athlete's Needs, Inc.
• UNII:
  • 9TN87S3A3C
• RxNorm Concept Unique ID - RxCUI:
  • 849574
• UPC Code:
  • 0092617374506

NDC Crossover Matching brand name "Naproxen Sodium 220mg" or generic name "Naproxen Sodium 220mg"

NDC	Brand Name	Generic Name
53185-362	Naproxen Sodium 220mg	Naproxen Sodium 220mg
53185-394	Naproxen Sodium 220mg	Naproxen Sodium 220mg
53329-678	Naproxen Sodium 220mg	Naproxen Sodium
53329-688	Naproxen Sodium 220mg	Naproxen Sodium
69168-395	Naproxen Sodium 220mg	Naproxen Sodium 220mg
69197-394	Naproxen Sodium 220mg	Naproxen Sodium 220mg
69168-632	Naproxen Sodium	Naproxen Sodium 220mg