Package 49708-755-41
Brand: bromfenac 0.075%
Generic: bromfenacPackage Facts
Identity
Package NDC
49708-755-41
Digits Only
4970875541
Product NDC
49708-755
Description
1 POUCH in 1 CARTON (49708-755-41) / 1 BOTTLE, DROPPER in 1 POUCH / 5 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
Brand
bromfenac 0.075%
Generic
bromfenac
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "47dae14d-3f32-0889-e063-6294a90aa707", "openfda": {"unii": ["8ECV571Y37"], "rxcui": ["1790141"], "spl_set_id": ["7d723a00-4822-4e04-aa22-21de22009d0a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (49708-755-41) / 1 BOTTLE, DROPPER in 1 POUCH / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "49708-755-41", "marketing_start_date": "20240207"}], "brand_name": "bromfenac 0.075%", "product_id": "49708-755_47dae14d-3f32-0889-e063-6294a90aa707", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49708-755", "generic_name": "bromfenac", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bromfenac", "brand_name_suffix": "0.075%", "active_ingredients": [{"name": "BROMFENAC SODIUM", "strength": ".76 mg/mL"}], "application_number": "NDA206911", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240207", "listing_expiration_date": "20271231"}