Package 70069-491-01
Brand: olopatadine hydrochloride
Generic: olopatadine hydrochloridePackage 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
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"}