Package 68180-436-01
Brand: bromfenac
Generic: bromfenacPackage Facts
Identity
Package NDC
68180-436-01
Digits Only
6818043601
Product NDC
68180-436
Description
1 BOTTLE in 1 CARTON (68180-436-01) / 1.7 mL in 1 BOTTLE
Marketing
Marketing Status
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": "8df89f04-52dd-4d9c-8cf3-9c045e669463", "openfda": {"unii": ["8ECV571Y37"], "rxcui": ["578018"], "spl_set_id": ["2fc689b7-d5ba-4591-8c23-b48e588d7a28"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68180-436-01) / 1.7 mL in 1 BOTTLE", "package_ndc": "68180-436-01", "marketing_start_date": "20240202"}], "brand_name": "Bromfenac", "product_id": "68180-436_8df89f04-52dd-4d9c-8cf3-9c045e669463", "dosage_form": "SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68180-436", "generic_name": "Bromfenac", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bromfenac", "active_ingredients": [{"name": "BROMFENAC SODIUM", "strength": ".9 mg/mL"}], "application_number": "ANDA202903", "marketing_category": "ANDA", "marketing_start_date": "20240202", "listing_expiration_date": "20261231"}