Package 0904-6966-61

Brand: oxycodone hydrochloride

Generic: oxycodone
NDC Package

Package Facts

Identity

Package NDC 0904-6966-61
Digits Only 0904696661
Product NDC 0904-6966
Product ID 0904-6966_9059237f-b963-405f-8988-4f50981a4260
Description

100 BLISTER PACK in 1 CARTON (0904-6966-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-10-30
Brand oxycodone hydrochloride
Generic oxycodone
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": "9059237f-b963-405f-8988-4f50981a4260", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049621"], "spl_set_id": ["6b6db42b-9821-4aa6-8566-297037d84079"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6966-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6966-61", "marketing_start_date": "20121030"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "0904-6966_9059237f-b963-405f-8988-4f50981a4260", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0904-6966", "dea_schedule": "CII", "generic_name": "Oxycodone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}