Package 24208-508-01

Brand: loteprednol etabonate

Generic: loteprednol etabonate
NDC Package

Package Facts

Identity

Package NDC 24208-508-01
Digits Only 2420850801
Product NDC 24208-508
Description

1 BOTTLE in 1 CARTON (24208-508-01) / 5 g in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-02-17
Brand loteprednol etabonate
Generic loteprednol etabonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "0cdbef52-3996-4d79-85ae-c5dd70ac93ed", "openfda": {"unii": ["YEH1EZ96K6"], "rxcui": ["1312625"], "spl_set_id": ["7bbdbd31-5a8f-4d69-aa8e-5b700895e804"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (24208-508-01)  / 5 g in 1 BOTTLE", "package_ndc": "24208-508-01", "marketing_start_date": "20210217"}], "brand_name": "Loteprednol Etabonate", "product_id": "24208-508_0cdbef52-3996-4d79-85ae-c5dd70ac93ed", "dosage_form": "GEL", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "24208-508", "generic_name": "loteprednol etabonate", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loteprednol Etabonate", "active_ingredients": [{"name": "LOTEPREDNOL ETABONATE", "strength": "5 mg/g"}], "application_number": "NDA202872", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20210217", "listing_expiration_date": "20261231"}