Package 0093-0314-01

Brand: ketorolac tromethamine

Generic: ketorolac tromethamine
NDC Package

Package Facts

Identity

Package NDC 0093-0314-01
Digits Only 0093031401
Product NDC 0093-0314
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-0314-01)

Marketing

Marketing Status
Marketed Since 1998-06-17
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": "06cd0a02-e137-4ae7-9f76-a416efe1f191", "openfda": {"unii": ["4EVE5946BQ"], "rxcui": ["834022"], "spl_set_id": ["688f5dec-a6db-43c6-a1f8-5df99d08d395"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0314-01)", "package_ndc": "0093-0314-01", "marketing_start_date": "19980617"}], "brand_name": "Ketorolac Tromethamine", "product_id": "0093-0314_06cd0a02-e137-4ae7-9f76-a416efe1f191", "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": "0093-0314", "generic_name": "Ketorolac Tromethamine", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketorolac Tromethamine", "active_ingredients": [{"name": "KETOROLAC TROMETHAMINE", "strength": "10 mg/1"}], "application_number": "ANDA074754", "marketing_category": "ANDA", "marketing_start_date": "19980617", "listing_expiration_date": "20261231"}