Package 80539-001-39

Brand: olopatadine hydrochloride

Generic: olopatadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80539-001-39
Digits Only 8053900139
Product NDC 80539-001
Description

1 BOTTLE, PLASTIC in 1 CARTON (80539-001-39) / 2.5 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2020-07-15
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": "12d48ef6-ccf1-4bc3-8469-0061bb083f7c", "openfda": {"unii": ["2XG66W44KF"], "rxcui": ["1111343"], "spl_set_id": ["12d48ef6-ccf1-4bc3-8469-0061bb083f7c"], "manufacturer_name": ["Allwell Health Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (80539-001-39)  / 2.5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "80539-001-39", "marketing_start_date": "20200715"}], "brand_name": "OLOPATADINE HYDROCHLORIDE", "product_id": "80539-001_12d48ef6-ccf1-4bc3-8469-0061bb083f7c", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Histamine Release [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Inhibitor [EPC]"], "product_ndc": "80539-001", "generic_name": "OLOPATADINE HYDROCHLORIDE", "labeler_name": "Allwell Health Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OLOPATADINE HYDROCHLORIDE", "active_ingredients": [{"name": "OLOPATADINE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA209995", "marketing_category": "ANDA", "marketing_start_date": "20200715", "listing_expiration_date": "20261231"}