Package 68094-005-61

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68094-005-61
Digits Only 6809400561
Product NDC 68094-005
Product ID 68094-005_31203769-a951-4d0c-8d60-4cb7715e26e8
Description

10 BLISTER PACK in 1 CARTON (68094-005-61) / 10 TABLET in 1 BLISTER PACK (68094-005-59)

Marketing

Marketing Status
Marketed Since 2016-12-21
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Morphine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "31203769-a951-4d0c-8d60-4cb7715e26e8", "openfda": {"upc": ["0368094005616"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["f849c7cc-fa85-47eb-be30-1be137913bf9"], "manufacturer_name": ["Precision Dose, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68094-005-61)  / 10 TABLET in 1 BLISTER PACK (68094-005-59)", "package_ndc": "68094-005-61", "marketing_start_date": "20161221"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "68094-005_31203769-a951-4d0c-8d60-4cb7715e26e8", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68094-005", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20161221", "listing_expiration_date": "20261231"}