Package 55700-174-90

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55700-174-90
Digits Only 5570017490
Product NDC 55700-174
Description

90 TABLET in 1 BOTTLE (55700-174-90)

Marketing

Marketing Status
Discontinued 2027-07-31
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dd30b87d-7f9b-43b8-b32e-c4d2937d6931", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618"], "spl_set_id": ["4cadb809-157d-49cc-97b4-3276594f19d2"], "manufacturer_name": ["Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (55700-174-30)", "package_ndc": "55700-174-30", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55700-174-60)", "package_ndc": "55700-174-60", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55700-174-90)", "package_ndc": "55700-174-90", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "55700-174_dd30b87d-7f9b-43b8-b32e-c4d2937d6931", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "55700-174", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "Quality Care Products LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}