Package 0093-0058-05

Brand: Tramadol Hydrochloride

Generic: Tramadol Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-0058-05
Digits Only 0093005805
Product NDC 0093-0058
Product ID 0093-0058_406611bf-17cb-4c5c-8921-1f3203b79d81
Description

500 TABLET, FILM COATED in 1 BOTTLE (0093-0058-05)

Marketing

Marketing Status
Discontinued 2026-02-28
Brand Tramadol Hydrochloride
Generic Tramadol Hydrochloride
Sample Package No

Linked Drug Pages (1)

Tramadol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "406611bf-17cb-4c5c-8921-1f3203b79d81", "openfda": {"upc": ["0300930058011"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["6d3b4049-2bfd-4874-b984-8fb231bff27c"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-0058-05)", "package_ndc": "0093-0058-05", "marketing_end_date": "20260228", "marketing_start_date": "20020703"}], "brand_name": "Tramadol Hydrochloride", "product_id": "0093-0058_406611bf-17cb-4c5c-8921-1f3203b79d81", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0093-0058", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075977", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20020620"}