OLOPATADINE HYDROCHLORIDE - olopatadine hydrochloride solution 
Amerisource Bergen

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Drug Facts

Active ingredient
Olopatadine (0.1%).
(equivalent to olopatadine hydrochloride, USP 0.111%)

Purpose

Antihistamine and Redness Reliever

Uses

temporarily relieves itchy and red eyes due to pollen, ragweed, grass, animal hair and dander

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if you experience:

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

    consult a doctor

Other information

Inactive ingredients

benzalkonium chloride 0.01%, dibasic sodium phosphate, hydrochloric acid/sodium hydroxide (adjust pH), sodium chloride and water for injection

Questions?

✆1-855-274-4122

Distributed by
AmerisourceBergen
1 West First Avenue
Conshohocken, PA 19428

Made in India
Code: TS/DRUGS/13/2010

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.1% (5 mL Container)

GOOD
NEIGHBOR
PHARMACY®                             NDC 46122-672-64

Olopatadine Hydrochloride
Ophthalmic Solution USP, 0.1%
Antihistamine and Redness Reliever
                         Eye Allergy Itch & Redness Relief
STERILE                                    5 mL (0.17 FL OZ)
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.1% (5 mL Container)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.1% (5 mL Container Carton)

                                                  *Compare to the Active Ingredient
                                                      in Pataday® Twice Daily Relief


GOOD
NEIGHBOR
PHARMACY®                             NDC 46122-672-64
NOW AVAILABLE without a prescription
Olopatadine Hydrochloride
Ophthalmic Solution, USP
0.1%
Antihistamine and Redness Reliever
                         Eye Allergy Itch & Redness Relief
Works in Minutes
Relief from Allergens:
• Pet Dander • Pollen                     TWICE
• Grass • Ragweed                          DAILY
STERILE
5 mL (0.17 FL OZ)
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.1% (5 mL Container Carton)

OLOPATADINE HYDROCHLORIDE 
olopatadine hydrochloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-672
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OLOPATADINE HYDROCHLORIDE (UNII: 2XG66W44KF) (OLOPATADINE - UNII:D27V6190PM) OLOPATADINE HYDROCHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-672-641 in 1 CARTON01/20/2021
15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20481201/20/2021
Labeler - Amerisource Bergen (007914906)
Registrant - Aurobindo Pharma Limited (650082092)
Establishment
NameAddressID/FEIBusiness Operations
Eugia Pharma Specialities Limited650498244ANALYSIS(46122-672) , MANUFACTURE(46122-672)

Revised: 7/2023
Document Id: 7420f7f2-f791-4d48-8f17-a9916bd8aa4b
Set id: f3b054d2-4abd-4a1f-910d-0c61e2a24fbf
Version: 4
Effective Time: 20230710
 
Amerisource Bergen