Package 76420-136-30

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 76420-136-30
Digits Only 7642013630
Product NDC 76420-136
Product ID 76420-136_ca9b9e11-ae8f-f35e-e053-2a95a90a8762
Description

30 TABLET in 1 BOTTLE (76420-136-30)

Marketing

Marketing Status
Marketed Since 2021-08-28
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": "ca9b9e11-ae8f-f35e-e053-2a95a90a8762", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049221"], "spl_set_id": ["0dcb491a-54e8-486b-9575-788525a178cf"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-136-30)", "package_ndc": "76420-136-30", "marketing_start_date": "20210828"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "76420-136_ca9b9e11-ae8f-f35e-e053-2a95a90a8762", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-136", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Asclemed USA, Inc.", "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": "ANDA201278", "marketing_category": "ANDA", "marketing_start_date": "20140828", "listing_expiration_date": "20261231"}