Package 42858-002-10

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42858-002-10
Digits Only 4285800210
Product NDC 42858-002
Product ID 42858-002_f1c3bf11-f460-43bf-9593-ed80fadcd317
Description

10 BLISTER PACK in 1 CARTON (42858-002-10) / 10 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-09-08
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f1c3bf11-f460-43bf-9593-ed80fadcd317", "openfda": {"upc": ["0342858002011", "0342858004015"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["a5162476-1217-41c0-bc7e-0a0f123f069f"], "manufacturer_name": ["Rhodes Pharmaceuticals L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (42858-002-01)", "package_ndc": "42858-002-01", "marketing_start_date": "20140908"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (42858-002-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "42858-002-10", "marketing_start_date": "20140908"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "42858-002_f1c3bf11-f460-43bf-9593-ed80fadcd317", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42858-002", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Rhodes Pharmaceuticals L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20271231"}