Package 70069-491-01

Brand: olopatadine hydrochloride

Generic: olopatadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-491-01
Digits Only 7006949101
Product NDC 70069-491
Description

2.5 mL in 1 BOTTLE, PLASTIC (70069-491-01)

Marketing

Marketing Status
Marketed Since 2024-12-20
Brand olopatadine hydrochloride
Generic olopatadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "f19c5298-b566-4416-a345-c5334c6a7ad7", "openfda": {"unii": ["2XG66W44KF"], "rxcui": ["1111343"], "spl_set_id": ["6ee9f8f5-973c-4c71-8069-e76cd87b07dc"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2.5 mL in 1 BOTTLE, PLASTIC (70069-491-01)", "package_ndc": "70069-491-01", "marketing_start_date": "20241220"}], "brand_name": "OLOPATADINE HYDROCHLORIDE", "product_id": "70069-491_f19c5298-b566-4416-a345-c5334c6a7ad7", "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": "70069-491", "generic_name": "Olopatadine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OLOPATADINE HYDROCHLORIDE", "active_ingredients": [{"name": "OLOPATADINE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA215006", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20261231"}