bromfenac sodium
Generic: bromfenac sodium
Labeler: alembic pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
bromfenac sodium
Generic Name
bromfenac sodium
Labeler
alembic pharmaceuticals inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
bromfenac sodium .805 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
62332-583
Product ID
62332-583_e680d513-20c9-4595-a293-d3f57d24f428
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214340
Listing Expiration
2026-12-31
Marketing Start
2024-07-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62332583
Hyphenated Format
62332-583
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 sodium (source: ndc)
Generic Name
bromfenac sodium (source: ndc)
Application Number
ANDA214340 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .805 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (62332-583-03) / 3 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": "e680d513-20c9-4595-a293-d3f57d24f428", "openfda": {"unii": ["8ECV571Y37"], "rxcui": ["1375917"], "spl_set_id": ["f6911061-d00e-466d-b623-f81730f38f98"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (62332-583-03) / 3 mL in 1 BOTTLE", "package_ndc": "62332-583-03", "marketing_start_date": "20240708"}], "brand_name": "BROMFENAC SODIUM", "product_id": "62332-583_e680d513-20c9-4595-a293-d3f57d24f428", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "62332-583", "generic_name": "BROMFENAC SODIUM", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BROMFENAC SODIUM", "active_ingredients": [{"name": "BROMFENAC SODIUM", "strength": ".805 mg/mL"}], "application_number": "ANDA214340", "marketing_category": "ANDA", "marketing_start_date": "20240708", "listing_expiration_date": "20261231"}