Package 68084-710-01

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 68084-710-01
Digits Only 6808471001
Product NDC 68084-710
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-710-01) / 1 TABLET in 1 BLISTER PACK (68084-710-11)

Marketing

Marketing Status
Marketed Since 2014-06-04
Brand oxycodone and acetaminophen
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1cfe716a-f97c-7f6f-e063-6394a90ad63c", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049225"], "spl_set_id": ["03c9ff0d-46e8-448c-944a-7ad59d1afd6d"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-710-01)  / 1 TABLET in 1 BLISTER PACK (68084-710-11)", "package_ndc": "68084-710-01", "marketing_start_date": "20140604"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "68084-710_1cfe716a-f97c-7f6f-e063-6394a90ad63c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68084-710", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202677", "marketing_category": "ANDA", "marketing_start_date": "20140604", "listing_expiration_date": "20261231"}