Package 68788-8701-2
Brand: ketorolac tromethamine
Generic: ketorolac tromethaminePackage Facts
Identity
Package NDC
68788-8701-2
Digits Only
6878887012
Product NDC
68788-8701
Description
20 TABLET, FILM COATED in 1 BOTTLE (68788-8701-2)
Marketing
Marketing Status
Brand
ketorolac tromethamine
Generic
ketorolac tromethamine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21939d3c-8c76-4298-9f6d-d5729168de71", "openfda": {"unii": ["4EVE5946BQ"], "rxcui": ["834022"], "spl_set_id": ["337afb4f-789f-4cac-817a-e4286664a71e"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8701-2)", "package_ndc": "68788-8701-2", "marketing_start_date": "20240627"}], "brand_name": "Ketorolac Tromethamine", "product_id": "68788-8701_21939d3c-8c76-4298-9f6d-d5729168de71", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitor [EPC]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8701", "generic_name": "Ketorolac Tromethamine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketorolac Tromethamine", "active_ingredients": [{"name": "KETOROLAC TROMETHAMINE", "strength": "10 mg/1"}], "application_number": "ANDA216759", "marketing_category": "ANDA", "marketing_start_date": "20240627", "listing_expiration_date": "20261231"}