Package 68682-732-05

Brand: fluorescein sodium and benoxinate hydrochloride

Generic: fluorescein sodium and benoxinate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68682-732-05
Digits Only 6868273205
Product NDC 68682-732
Description

1 BOTTLE, GLASS in 1 CARTON (68682-732-05) / 5 mL in 1 BOTTLE, GLASS

Marketing

Marketing Status
Discontinued 2026-04-30
Brand fluorescein sodium and benoxinate hydrochloride
Generic fluorescein sodium and benoxinate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "4bd52cd8-0105-2d1a-e063-6394a90a3819", "openfda": {"unii": ["0VE4U49K15", "93X55PE38X"], "rxcui": ["2287005"], "spl_set_id": ["580c7f94-7013-4b7a-9010-4d37186f5758"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (68682-732-05)  / 5 mL in 1 BOTTLE, GLASS", "package_ndc": "68682-732-05", "marketing_end_date": "20260430", "marketing_start_date": "20210325"}], "brand_name": "Fluorescein Sodium and Benoxinate Hydrochloride", "product_id": "68682-732_4bd52cd8-0105-2d1a-e063-6394a90a3819", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Diagnostic Dye [EPC]", "Dyes [MoA]"], "product_ndc": "68682-732", "generic_name": "Fluorescein Sodium and Benoxinate Hydrochloride", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluorescein Sodium and Benoxinate Hydrochloride", "active_ingredients": [{"name": "BENOXINATE HYDROCHLORIDE", "strength": "4.4 mg/mL"}, {"name": "FLUORESCEIN SODIUM", "strength": "2.6 mg/mL"}], "application_number": "NDA211039", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260430", "marketing_start_date": "20210325"}