Package 60687-642-01

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 60687-642-01
Digits Only 6068764201
Product NDC 60687-642
Product ID 60687-642_446cc62f-293a-f35e-e063-6294a90a7dd0
Description

100 BLISTER PACK in 1 CARTON (60687-642-01) / 1 TABLET in 1 BLISTER PACK (60687-642-11)

Marketing

Marketing Status
Marketed Since 2022-01-04
Brand oxycodone and acetaminophen
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

Oxycodone and Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "446cc62f-293a-f35e-e063-6294a90a7dd0", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049221"], "spl_set_id": ["79bb61d7-8836-4ce7-91bc-9463efbad9cf"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-642-01)  / 1 TABLET in 1 BLISTER PACK (60687-642-11)", "package_ndc": "60687-642-01", "marketing_start_date": "20220104"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "60687-642_446cc62f-293a-f35e-e063-6294a90a7dd0", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60687-642", "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": "5 mg/1"}], "application_number": "ANDA207510", "marketing_category": "ANDA", "marketing_start_date": "20220104", "listing_expiration_date": "20261231"}