Package 68180-434-01

Brand: bromfenac

Generic: bromfenac
NDC Package

Package Facts

Identity

Package NDC 68180-434-01
Digits Only 6818043401
Product NDC 68180-434
Description

1 BOTTLE in 1 CARTON (68180-434-01) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-02-12
Brand bromfenac
Generic bromfenac
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "bde2565a-075e-4910-874b-9737d0ed9ccc", "openfda": {"unii": ["8ECV571Y37"], "rxcui": ["1790141"], "spl_set_id": ["2b2621e7-a69e-4286-a7e7-0fc31a91fe29"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68180-434-01)  / 5 mL in 1 BOTTLE", "package_ndc": "68180-434-01", "marketing_start_date": "20240212"}], "brand_name": "BROMFENAC", "product_id": "68180-434_bde2565a-075e-4910-874b-9737d0ed9ccc", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68180-434", "generic_name": "BROMFENAC", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BROMFENAC", "active_ingredients": [{"name": "BROMFENAC SODIUM", "strength": ".75 mg/mL"}], "application_number": "ANDA211239", "marketing_category": "ANDA", "marketing_start_date": "20240212", "listing_expiration_date": "20261231"}