Package 70710-1710-1

Brand: ketorolac tromethamine

Generic: ketorolac tromethamine
NDC Package

Package Facts

Identity

Package NDC 70710-1710-1
Digits Only 7071017101
Product NDC 70710-1710
Description

100 TABLET, FILM COATED in 1 BOTTLE (70710-1710-1)

Marketing

Marketing Status
Marketed Since 2022-11-10
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": "80144a41-dfe6-4ba9-bb1b-f846873043ea", "openfda": {"unii": ["4EVE5946BQ"], "rxcui": ["834022"], "spl_set_id": ["ffd84ef3-26ed-4810-952b-4f0e913c5e32"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1710-1)", "package_ndc": "70710-1710-1", "marketing_start_date": "20221110"}], "brand_name": "ketorolac tromethamine", "product_id": "70710-1710_80144a41-dfe6-4ba9-bb1b-f846873043ea", "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": "70710-1710", "generic_name": "ketorolac tromethamine", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ketorolac tromethamine", "active_ingredients": [{"name": "KETOROLAC TROMETHAMINE", "strength": "10 mg/1"}], "application_number": "ANDA217038", "marketing_category": "ANDA", "marketing_start_date": "20221110", "listing_expiration_date": "20261231"}