bromsite 0.075%
Generic: bromfenac
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
bromsite 0.075%
Generic Name
bromfenac
Labeler
sun pharmaceutical industries, inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
bromfenac sodium .76 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
49708-754
Product ID
49708-754_47daa628-c56f-1e9d-e063-6294a90a3d33
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA206911
Listing Expiration
2027-12-31
Marketing Start
2016-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49708754
Hyphenated Format
49708-754
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
bromsite 0.075% (source: ndc)
Generic Name
bromfenac (source: ndc)
Application Number
NDA206911 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .76 mg/mL
Packaging
- 1 POUCH in 1 CARTON (49708-754-41) / 1 BOTTLE, DROPPER in 1 POUCH / 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": "47daa628-c56f-1e9d-e063-6294a90a3d33", "openfda": {"unii": ["8ECV571Y37"], "rxcui": ["1790141", "1790146"], "spl_set_id": ["144a5072-341b-4591-8705-773b63044bcc"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (49708-754-41) / 1 BOTTLE, DROPPER in 1 POUCH / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "49708-754-41", "marketing_start_date": "20160501"}], "brand_name": "BROMSITE 0.075%", "product_id": "49708-754_47daa628-c56f-1e9d-e063-6294a90a3d33", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49708-754", "generic_name": "bromfenac", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BROMSITE", "brand_name_suffix": "0.075%", "active_ingredients": [{"name": "BROMFENAC SODIUM", "strength": ".76 mg/mL"}], "application_number": "NDA206911", "marketing_category": "NDA", "marketing_start_date": "20160501", "listing_expiration_date": "20271231"}