Package 58602-745-14
Brand: acetaminophen extra strength
Generic: acetaminophenPackage Facts
Identity
Package NDC
58602-745-14
Digits Only
5860274514
Product NDC
58602-745
Description
1 BOTTLE in 1 CARTON (58602-745-14) / 50 TABLET in 1 BOTTLE
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": "0b44d6cf-d21e-741a-e063-6294a90a05ff", "openfda": {"unii": ["362O9ITL9D"], "spl_set_id": ["bc03fa56-8880-4bbd-81a0-91853fecdd4e"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-07) / 24 TABLET in 1 BOTTLE", "package_ndc": "58602-745-07", "marketing_start_date": "20210107"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-14) / 50 TABLET in 1 BOTTLE", "package_ndc": "58602-745-14", "marketing_start_date": "20210107"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-21) / 100 TABLET in 1 BOTTLE", "package_ndc": "58602-745-21", "marketing_start_date": "20210107"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-35) / 225 TABLET in 1 BOTTLE", "package_ndc": "58602-745-35", "marketing_start_date": "20210107"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "58602-745_0b44d6cf-d21e-741a-e063-6294a90a05ff", "dosage_form": "TABLET", "product_ndc": "58602-745", "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": "20210107", "listing_expiration_date": "20261231"}