NAPROXEN SODIUM - naproxen sodium tablet, film coated 
Aurohealth LLC

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Naproxen Sodium Tablets, USP 220 mg

Drug Facts

Active ingredient (in each tablet)

Naproxen sodium USP 220 mg (naproxen 200 mg) (NSAID)*

*nonsteroidal anti-inflammatory drug

Purposes

Pain reliever/fever reducer

Uses

Warnings

Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:



If an allergic reaction occurs, stop use and seek medical help right away.

Stomach bleeding warning:
This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:


Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

Do not use

Ask a doctor before use if

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

ask a health professional before use. It is especially important not to use naproxen sodium at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions


 Adults and children
 12 years and older
  • take 1 tablet every 8 to 12 hours while symptoms last
  • for the first dose you may take 2 tablets within the first hour
  • do not exceed 2 tablets in any 8 to 12 hour period
  • do not exceed 3 tablets in a 24 hour period
 Children under 12 years
  • ask a doctor

Other information

Inactive ingredients

colloidal silicon dioxide, FD&C blue #2 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, talc, and titanium dioxide

Questions or comments?

1-855-274-4122

Distributed by: AUROHEALTH LLC
279 Princeton-Hightstown Road,
East Windsor, NJ 08520
Made in India

Code: TS/DRUGS/22/2009

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (100 Tablets Bottle)

AUROHEALTH
NDC 58602-819-21
Naproxen Sodium Tablets, USP
220 mg (NSAID)

STRENGTH TO LAST 12 HOURS
100
Tablets


PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (100 Tablet Bottle)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (100 Tablets Carton Label)

AUROHEALTH
NDC 58602-819-21
**Compare to Aleve®

active ingredient
Naproxen Sodium Tablets, USP
 220 mg (NSAID)

STRENGTH TO LAST 12 HOURS
100 Tablets

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (100 Tablets Carton Label)

NAPROXEN SODIUM 
naproxen sodium tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58602-819
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPROXEN SODIUM (UNII: 9TN87S3A3C) (NAPROXEN - UNII:57Y76R9ATQ) NAPROXEN SODIUM220 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
POVIDONE K30 (UNII: U725QWY32X)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorBLUE (light blue) Scoreno score
ShapeOVALSize12mm
FlavorImprint Code K;45
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58602-819-211 in 1 CARTON12/11/2017
1100 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:58602-819-141 in 1 CARTON12/11/2017
250 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:58602-819-071 in 1 CARTON10/25/2021
324 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:58602-819-291 in 1 CARTON10/25/2021
4150 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:58602-819-381 in 1 CARTON10/25/2021
5300 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:58602-819-401 in 1 CARTON10/25/2021
6500 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:58602-819-191 in 1 CARTON09/21/2023
790 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20549712/11/2017
Labeler - Aurohealth LLC (078728447)
Establishment
NameAddressID/FEIBusiness Operations
Aurobindo Pharma Limited650381903ANALYSIS(58602-819) , MANUFACTURE(58602-819)

Revised: 12/2023
Document Id: c1e447e8-3d9f-42b9-8ddc-c2e6b16700a8
Set id: 46a15412-25d6-454d-86db-70321d19a2c9
Version: 7
Effective Time: 20231215
 
Aurohealth LLC