Package 72189-376-60
Brand: acetaminophen and codeine phosphate
Generic: acetaminophen and codeine phosphatePackage Facts
Identity
Package NDC
72189-376-60
Digits Only
7218937660
Product NDC
72189-376
Description
60 TABLET in 1 BOTTLE (72189-376-60)
Marketing
Marketing Status
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": "2c4cbd73-cdae-14f5-e063-6294a90ab38e", "openfda": {"unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993890"], "spl_set_id": ["e78e50c0-36da-528e-e053-2995a90a3d80"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-376-60)", "package_ndc": "72189-376-60", "marketing_start_date": "20220831"}], "brand_name": "Acetaminophen and Codeine Phosphate", "product_id": "72189-376_2c4cbd73-cdae-14f5-e063-6294a90ab38e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-376", "dea_schedule": "CIII", "generic_name": "Acetaminophen and Codeine Phosphate", "labeler_name": "Direct_Rx", "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": "ANDA040419", "marketing_category": "ANDA", "marketing_start_date": "20220831", "listing_expiration_date": "20261231"}