flurbiprofen sodium
Generic: flurbiprofen sodium
Labeler: bausch & lomb incorporatedDrug Facts
Product Profile
Brand Name
flurbiprofen sodium
Generic Name
flurbiprofen sodium
Labeler
bausch & lomb incorporated
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
flurbiprofen sodium .3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24208-314
Product ID
24208-314_1e00e938-a04a-4192-e063-6394a90a75a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074447
Listing Expiration
2026-12-31
Marketing Start
1995-01-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24208314
Hyphenated Format
24208-314
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
flurbiprofen sodium (source: ndc)
Generic Name
flurbiprofen sodium (source: ndc)
Application Number
ANDA074447 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .3 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (24208-314-25) / 2.5 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
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"}