Package 58602-746-44
Brand: acetaminophen extra strength
Generic: acetaminophenPackage Facts
Identity
Package NDC
58602-746-44
Digits Only
5860274644
Product NDC
58602-746
Description
400 TABLET in 1 BOTTLE (58602-746-44)
Marketing
Marketing Status
Brand
acetaminophen extra strength
Generic
acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b451b78-386d-5ec1-e063-6394a90a79a7", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["03d42892-4465-4089-90a7-cd5f00c35602"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET in 1 BOTTLE (58602-746-44)", "package_ndc": "58602-746-44", "marketing_start_date": "20220218"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "58602-746_0b451b78-386d-5ec1-e063-6394a90a79a7", "dosage_form": "TABLET", "product_ndc": "58602-746", "generic_name": "Acetaminophen", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220218", "listing_expiration_date": "20261231"}