eye allergy itch relief

Generic: olopatadine hydrochloride

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name eye allergy itch relief
Generic Name olopatadine hydrochloride
Labeler cardinal health 110, llc. dba leader
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

olopatadine hydrochloride 7 mg/mL

Manufacturer
CARDINAL HEALTH 110, LLC. DBA LEADER

Identifiers & Regulatory

Product NDC 70000-0746
Product ID 70000-0746_8a98a890-5508-2451-1958-88e07eee2ccf
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213514
Listing Expiration 2027-12-31
Marketing Start 2026-01-15

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 700000746
Hyphenated Format 70000-0746

Supplemental Identifiers

RxCUI
1601086
UNII
2XG66W44KF

Packaging Origin

Original Packager
true

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 eye allergy itch relief (source: ndc)
Generic Name olopatadine hydrochloride (source: ndc)
Application Number ANDA213514 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 7 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (70000-0746-1) / 2.5 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

Ingredients (1)

olopatadine hydrochloride (7 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "8a98a890-5508-2451-1958-88e07eee2ccf", "openfda": {"unii": ["2XG66W44KF"], "rxcui": ["1601086"], "spl_set_id": ["5d79fc06-a25f-debb-f08b-523ff26df900"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (70000-0746-1)  / 2.5 mL in 1 BOTTLE, DROPPER", "package_ndc": "70000-0746-1", "marketing_start_date": "20260115"}], "brand_name": "Eye Allergy Itch Relief", "product_id": "70000-0746_8a98a890-5508-2451-1958-88e07eee2ccf", "dosage_form": "SOLUTION/ DROPS", "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": "70000-0746", "generic_name": "olopatadine hydrochloride", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eye Allergy Itch Relief", "active_ingredients": [{"name": "OLOPATADINE HYDROCHLORIDE", "strength": "7 mg/mL"}], "application_number": "ANDA213514", "marketing_category": "ANDA", "marketing_start_date": "20260115", "listing_expiration_date": "20271231"}