bromfenac
Generic: bromfenac
Labeler: lupin pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
bromfenac
Generic Name
bromfenac
Labeler
lupin pharmaceuticals, inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
bromfenac sodium .75 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68180-434
Product ID
68180-434_bde2565a-075e-4910-874b-9737d0ed9ccc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211239
Listing Expiration
2026-12-31
Marketing Start
2024-02-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68180434
Hyphenated Format
68180-434
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
bromfenac (source: ndc)
Generic Name
bromfenac (source: ndc)
Application Number
ANDA211239 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .75 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (68180-434-01) / 5 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
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"}