olopatadine hydrochloride ophthalmic solution (21130-105)

Drug Facts

Product Profile

Brand Name olopatadine hydrochloride ophthalmic solution

Generic Name olopatadine hydrochloride ophthalmic

Labeler albertsons companies

Dosage Form SOLUTION

Routes

OPHTHALMIC

Active Ingredients

olopatadine hydrochloride 2 mg/mL

Manufacturer

Albertsons Companies

Identifiers & Regulatory

Product NDC 21130-105

Product ID 21130-105_ac0a51c9-185a-9d58-cb21-ee5b6a1134d6

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209752

Listing Expiration 2026-12-31

Marketing Start 2021-06-25

Pharmacologic Class

Classes

decreased histamine release [pe] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] histamine-1 receptor inhibitor [epc] mast cell stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21130105

Hyphenated Format 21130-105

Supplemental Identifiers

RxCUI

1111343

UNII

2XG66W44KF

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name olopatadine hydrochloride ophthalmic solution (source: ndc)

Generic Name olopatadine hydrochloride ophthalmic (source: ndc)

Application Number ANDA209752 (source: ndc)

Routes

OPHTHALMIC

source: ndc

Resolved Composition

Strengths

2 mg/mL

source: ndc

Packaging

1 BOTTLE, PLASTIC in 1 CARTON (21130-105-02) / 2.5 mL in 1 BOTTLE, PLASTIC

source: ndc

Packages (1)

21130-105-02 1 BOTTLE, PLASTIC in 1 CARTON (21130-105-02) / 2.5 mL in 1 BOTTLE, PLASTIC

Ingredients (1)

olopatadine hydrochloride (2 mg/mL)

Linked Drug Pages (1)

Olopatadine Hydrochloride Ophthalmic Solution ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["OPHTHALMIC"], "spl_id": "ac0a51c9-185a-9d58-cb21-ee5b6a1134d6", "openfda": {"unii": ["2XG66W44KF"], "rxcui": ["1111343"], "spl_set_id": ["685192af-d729-3066-5825-6d0e03ce787e"], "manufacturer_name": ["Albertsons Companies"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (21130-105-02)  / 2.5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "21130-105-02", "marketing_start_date": "20210625"}], "brand_name": "Olopatadine Hydrochloride Ophthalmic Solution", "product_id": "21130-105_ac0a51c9-185a-9d58-cb21-ee5b6a1134d6", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Histamine Release [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Histamine-1 Receptor Inhibitor [EPC]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "21130-105", "generic_name": "Olopatadine Hydrochloride Ophthalmic", "labeler_name": "Albertsons Companies", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Olopatadine Hydrochloride Ophthalmic Solution", "active_ingredients": [{"name": "OLOPATADINE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA209752", "marketing_category": "ANDA", "marketing_start_date": "20210625", "listing_expiration_date": "20261231"}