Package 23635-582-10

Brand: roxicodone

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 23635-582-10
Digits Only 2363558210
Product NDC 23635-582
Product ID 23635-582_c4519228-edfd-422f-876d-b5edd5ff7283
Description

100 TABLET in 1 BOTTLE, PLASTIC (23635-582-10)

Marketing

Marketing Status
Marketed Since 2000-08-31
Brand roxicodone
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Roxicodone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4519228-edfd-422f-876d-b5edd5ff7283", "openfda": {"upc": ["0323635582100", "0323635581103"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049613", "1049618", "1049620"], "spl_set_id": ["5a8157d3-ba20-4abf-b0d4-6ad141b31d63"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (23635-582-10)", "package_ndc": "23635-582-10", "marketing_start_date": "20000831"}], "brand_name": "Roxicodone", "product_id": "23635-582_c4519228-edfd-422f-876d-b5edd5ff7283", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "23635-582", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Roxicodone", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA021011", "marketing_category": "NDA", "marketing_start_date": "20000831", "listing_expiration_date": "20261231"}