Package 68788-8891-2

Brand: ketorolac tromethamine

Generic: ketorolac tromethamine
NDC Package

Package Facts

Identity

Package NDC 68788-8891-2
Digits Only 6878888912
Product NDC 68788-8891
Description

20 TABLET, FILM COATED in 1 BOTTLE (68788-8891-2)

Marketing

Marketing Status
Marketed Since 2025-09-23
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": "18b450d2-e715-4710-a1d8-22b782f87f9c", "openfda": {"unii": ["4EVE5946BQ"], "rxcui": ["834022"], "spl_set_id": ["18b450d2-e715-4710-a1d8-22b782f87f9c"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8891-2)", "package_ndc": "68788-8891-2", "marketing_start_date": "20250923"}], "brand_name": "Ketorolac Tromethamine", "product_id": "68788-8891_18b450d2-e715-4710-a1d8-22b782f87f9c", "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": "68788-8891", "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": "ANDA215788", "marketing_category": "ANDA", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}