Package 68682-732-05
Brand: fluorescein sodium and benoxinate hydrochloride
Generic: fluorescein sodium and benoxinate hydrochloridePackage 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
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"}