Package 24208-314-25

Brand: flurbiprofen sodium

Generic: flurbiprofen sodium
NDC Package

Package Facts

Identity

Package NDC 24208-314-25
Digits Only 2420831425
Product NDC 24208-314
Description

1 BOTTLE, DROPPER in 1 CARTON (24208-314-25) / 2.5 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 1995-01-04
Brand flurbiprofen sodium
Generic flurbiprofen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "1e00e938-a04a-4192-e063-6394a90a75a6", "openfda": {"unii": ["Z5B97MU9K4"], "rxcui": ["1243585"], "spl_set_id": ["11db354f-caf9-4567-811e-6c9beb1330c7"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-314-25)  / 2.5 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-314-25", "marketing_start_date": "19950104"}], "brand_name": "Flurbiprofen Sodium", "product_id": "24208-314_1e00e938-a04a-4192-e063-6394a90a75a6", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "24208-314", "generic_name": "Flurbiprofen Sodium", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flurbiprofen Sodium", "active_ingredients": [{"name": "FLURBIPROFEN SODIUM", "strength": ".3 mg/mL"}], "application_number": "ANDA074447", "marketing_category": "ANDA", "marketing_start_date": "19950104", "listing_expiration_date": "20261231"}