Package 72162-2001-1

Brand: acetaminophen and codeine phosphate

Generic: acetaminophen and codeine phosphate
NDC Package

Package Facts

Identity

Package NDC 72162-2001-1
Digits Only 7216220011
Product NDC 72162-2001
Description

100 TABLET in 1 BOTTLE (72162-2001-1)

Marketing

Marketing Status
Marketed Since 2019-08-02
Brand acetaminophen and codeine phosphate
Generic acetaminophen and codeine phosphate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eea244e1-de1a-409b-8a19-6395eda056ad", "openfda": {"unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993781"], "spl_set_id": ["879db1b5-6365-4151-9879-80d8a2a3cd8a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2001-1)", "package_ndc": "72162-2001-1", "marketing_start_date": "20190802"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2001-5)", "package_ndc": "72162-2001-5", "marketing_start_date": "20190802"}], "brand_name": "ACETAMINOPHEN AND CODEINE PHOSPHATE", "product_id": "72162-2001_eea244e1-de1a-409b-8a19-6395eda056ad", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-2001", "dea_schedule": "CIII", "generic_name": "acetaminophen and codeine phosphate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACETAMINOPHEN AND CODEINE PHOSPHATE", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "CODEINE PHOSPHATE", "strength": "30 mg/1"}], "application_number": "ANDA211610", "marketing_category": "ANDA", "marketing_start_date": "20190802", "listing_expiration_date": "20261231"}