Package 71930-054-52

Brand: ACETAMINOPHEN AND CODEINE PHOSPHATE

Generic: acetaminophen and codeine phosphate
NDC Package

Package Facts

Identity

Package NDC 71930-054-52
Digits Only 7193005452
Product NDC 71930-054
Description

500 TABLET in 1 BOTTLE (71930-054-52)

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": "7570113f-54f9-4ce5-80b9-7c6811e49e34", "openfda": {"unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993770", "993781", "993890"], "spl_set_id": ["79377617-686b-4640-b2b8-e1358cf82358"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71930-054-12)", "package_ndc": "71930-054-12", "marketing_start_date": "20190802"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71930-054-52)", "package_ndc": "71930-054-52", "marketing_start_date": "20190802"}], "brand_name": "ACETAMINOPHEN AND CODEINE PHOSPHATE", "product_id": "71930-054_7570113f-54f9-4ce5-80b9-7c6811e49e34", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71930-054", "dea_schedule": "CII", "generic_name": "acetaminophen and codeine phosphate", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACETAMINOPHEN AND CODEINE PHOSPHATE", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "CODEINE PHOSPHATE", "strength": "15 mg/1"}], "application_number": "ANDA211610", "marketing_category": "ANDA", "marketing_start_date": "20190802", "listing_expiration_date": "20261231"}