IBUPROFEN - ibuprofen tablet 
Aurohealth LLC

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Ibuprofen Tablets

Drug Facts

Active ingredient (in each tablet)

Ibuprofen USP 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug

Purposes

Pain reliever/Fever reducer

Uses

Warnings

Allergy alert: Ibuprofen 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 ibuprofen 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 right away. (1-800-222-1222)

Directions

adults and children 12 years and older
  • take 1 tablet every 4 to 6 hours while symptoms persist
  • if pain or fever does not respond to 1 tablet, 2 tablets may be used
  • do not exceed 6 tablets in 24 hours, unless directed by a doctor
children under 12 years
  • ask a doctor

Other information

Inactive ingredients

colloidal silicon dioxide, corn starch, croscarmellose sodium, hypromellose, microcrystalline cellulose, polyethylene glycol, red iron oxide, stearic acid, titanium dioxide and yellow iron oxide

Questions or comments?

Call 1-855-274-4122

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

Made in India

Code: TS/DRUGS/16/2014


PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg (100 Tablets Bottle)

AUROHEALTH
NDC 58602-708-07
Ibuprofen Tablets USP
200 mg
Pain Reliever/Fever Reducer (NSAID)
100 Coated Tablets

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg (100 Tablet Bottle)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg (100 Tablets Container Carton)

AUROHEALTH
NDC 58602-708-07
#Compare to the active
ingredient of MOTRIN® IB
Ibuprofen Tablets USP
200 mg
Pain Reliever/Fever Reducer (NSAID)
100 Coated Tablets

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 200 mg (100 Tablets Container Carton)

IBUPROFEN 
ibuprofen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58602-708
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STARCH, CORN (UNII: O8232NY3SJ)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
Product Characteristics
ColorBROWN (Light Brown to Brown) Scoreno score
ShapeROUNDSize10mm
FlavorImprint Code N;II
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58602-708-731 in 1 CARTON03/22/2022
124 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:58602-708-091 in 1 CARTON03/22/2022
250 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:58602-708-071 in 1 CARTON03/22/2022
3100 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:58602-708-531 in 1 CARTON03/22/2022
4150 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:58602-708-831 in 1 CARTON03/22/2022
5200 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:58602-708-49300 in 1 BOTTLE; Type 0: Not a Combination Product03/22/2022
7NDC:58602-708-011 in 1 CARTON03/22/2022
724 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
8NDC:58602-708-051 in 1 CARTON03/22/2022
840 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
9NDC:58602-708-081 in 1 CARTON03/22/2022
950 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
10NDC:58602-708-151 in 1 CARTON03/22/2022
1060 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
11NDC:58602-708-061 in 1 CARTON03/22/2022
1190 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
12NDC:58602-708-021 in 1 CARTON03/22/2022
12100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
13NDC:58602-708-031 in 1 CARTON03/22/2022
13150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
14NDC:58602-708-04200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/22/2022
15NDC:58602-708-36250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/22/2022
16NDC:58602-708-75300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/22/2022
17NDC:58602-708-87550 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/22/2022
18NDC:58602-708-52700 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/22/2022
19NDC:58602-708-411000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/22/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20886503/22/2022
Labeler - Aurohealth LLC (078728447)
Establishment
NameAddressID/FEIBusiness Operations
APL HEALTHCARE LIMITED650844777ANALYSIS(58602-708) , MANUFACTURE(58602-708)
Establishment
NameAddressID/FEIBusiness Operations
Aurobindo Pharma Limited650381903ANALYSIS(58602-708) , MANUFACTURE(58602-708)

Revised: 3/2022
Document Id: 09bd3935-526d-4ad1-898a-4f0d9499ebb9
Set id: 09bd3935-526d-4ad1-898a-4f0d9499ebb9
Version: 1
Effective Time: 20220323
 
Aurohealth LLC