olopatadine hydrochloride
Generic: olopatadine hydrochloride
Labeler: retail business services, llc.Drug Facts
Product Profile
Brand Name
olopatadine hydrochloride
Generic Name
olopatadine hydrochloride
Labeler
retail business services, llc.
Dosage Form
SOLUTION
Routes
Active Ingredients
olopatadine hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72476-852
Product ID
72476-852_3de497ac-ef3e-4eb0-88e3-723394770274
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA204812
Listing Expiration
2026-12-31
Marketing Start
2021-05-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72476852
Hyphenated Format
72476-852
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Generic Name
olopatadine hydrochloride (source: ndc)
Application Number
ANDA204812 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (72476-852-64) / 5 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "3de497ac-ef3e-4eb0-88e3-723394770274", "openfda": {"unii": ["2XG66W44KF"], "rxcui": ["1111339"], "spl_set_id": ["bd2deb79-c135-2d3f-e053-2a95a90a9322"], "manufacturer_name": ["Retail Business Services, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-852-64) / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "72476-852-64", "marketing_start_date": "20210506"}], "brand_name": "OLOPATADINE HYDROCHLORIDE", "product_id": "72476-852_3de497ac-ef3e-4eb0-88e3-723394770274", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Histamine Release [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Inhibitor [EPC]"], "product_ndc": "72476-852", "generic_name": "OLOPATADINE HYDROCHLORIDE", "labeler_name": "Retail Business Services, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OLOPATADINE HYDROCHLORIDE", "active_ingredients": [{"name": "OLOPATADINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA204812", "marketing_category": "ANDA", "marketing_start_date": "20210506", "listing_expiration_date": "20261231"}