Package 71335-1473-1

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71335-1473-1
Digits Only 7133514731
Product NDC 71335-1473
Product ID 71335-1473_d20e2622-e1a1-45e8-a670-7bc76ed896e0
Description

21 TABLET in 1 BOTTLE (71335-1473-1)

Marketing

Marketing Status
Marketed Since 2022-02-09
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": "d20e2622-e1a1-45e8-a670-7bc76ed896e0", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049221"], "spl_set_id": ["c70d906d-2d7e-427b-9945-b75d2ab1681f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-1473-1)", "package_ndc": "71335-1473-1", "marketing_start_date": "20220209"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "71335-1473_d20e2622-e1a1-45e8-a670-7bc76ed896e0", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1473", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "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"}