Package 55700-984-30

Brand: OXYCODONE AND ACETAMINOPHEN

Generic: oxycodone hydrochloride and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 55700-984-30
Digits Only 5570098430
Product NDC 55700-984
Description

30 TABLET in 1 BOTTLE (55700-984-30)

Marketing

Marketing Status
Discontinued 2026-02-28
Brand OXYCODONE AND ACETAMINOPHEN
Generic oxycodone hydrochloride and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fdd71f8f-45de-44a3-8ccf-c9b9e42036bd", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["c33734a7-2abb-47f3-abeb-041a2c033225"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (55700-984-30)", "package_ndc": "55700-984-30", "marketing_end_date": "20260228", "marketing_start_date": "20220928"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55700-984-60)", "package_ndc": "55700-984-60", "marketing_end_date": "20260228", "marketing_start_date": "20220928"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55700-984-90)", "package_ndc": "55700-984-90", "marketing_end_date": "20260228", "marketing_start_date": "20220928"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "55700-984_fdd71f8f-45de-44a3-8ccf-c9b9e42036bd", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "55700-984", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride and acetaminophen", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA040545", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20220928"}