olopatadine hydrochloride

Generic: olopatadine hydrochloride

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olopatadine hydrochloride
Generic Name olopatadine hydrochloride
Labeler rising pharma holdings, inc.
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

olopatadine hydrochloride 1 mg/mL

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-882
Product ID 16571-882_c23fbb1d-8ba4-4375-aedf-f2346dde7746
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204392
Listing Expiration 2026-12-31
Marketing Start 2025-05-01

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 16571882
Hyphenated Format 16571-882

Supplemental Identifiers

RxCUI
1111339
UPC
0316571882052
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 olopatadine hydrochloride (source: ndc)
Generic Name olopatadine hydrochloride (source: ndc)
Application Number ANDA204392 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 CONTAINER in 1 CARTON (16571-882-05) / 5 mL in 1 CONTAINER
source: ndc

Packages (1)

Ingredients (1)

olopatadine hydrochloride (1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "c23fbb1d-8ba4-4375-aedf-f2346dde7746", "openfda": {"upc": ["0316571882052"], "unii": ["2XG66W44KF"], "rxcui": ["1111339"], "spl_set_id": ["7c86e2d4-2d37-4ccf-9227-820a50637778"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CONTAINER in 1 CARTON (16571-882-05)  / 5 mL in 1 CONTAINER", "package_ndc": "16571-882-05", "marketing_start_date": "20250501"}], "brand_name": "olopatadine hydrochloride", "product_id": "16571-882_c23fbb1d-8ba4-4375-aedf-f2346dde7746", "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": "16571-882", "generic_name": "olopatadine hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "olopatadine hydrochloride", "active_ingredients": [{"name": "OLOPATADINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA204392", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}