Package 72162-2002-5

Brand: acetaminophen and codeine phosphate

Generic: acetaminophen and codeine phosphate
NDC Package

Package Facts

Identity

Package NDC 72162-2002-5
Digits Only 7216220025
Product NDC 72162-2002
Description

500 TABLET in 1 BOTTLE (72162-2002-5)

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": "142a0710-5937-436f-98cb-de31791f0f8e", "openfda": {"unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993890"], "spl_set_id": ["e73b17c4-9f24-4b32-8920-61c58c40a714"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2002-1)", "package_ndc": "72162-2002-1", "marketing_start_date": "20190802"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2002-5)", "package_ndc": "72162-2002-5", "marketing_start_date": "20190802"}], "brand_name": "ACETAMINOPHEN AND CODEINE PHOSPHATE", "product_id": "72162-2002_142a0710-5937-436f-98cb-de31791f0f8e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-2002", "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": "60 mg/1"}], "application_number": "ANDA211610", "marketing_category": "ANDA", "marketing_start_date": "20190802", "listing_expiration_date": "20261231"}