Package 58602-771-64
Brand: aurophen extra strength for adults
Generic: acetaminophenPackage Facts
Identity
Package NDC
58602-771-64
Digits Only
5860277164
Product NDC
58602-771
Description
600 TABLET in 1 BOTTLE (58602-771-64)
Marketing
Marketing Status
Brand
aurophen extra strength for adults
Generic
acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b45ad4e-d9d9-d463-e063-6294a90a195d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["d59c5f04-4bcc-4a52-a42f-e049506f00de"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET in 1 BOTTLE (58602-771-36)", "package_ndc": "58602-771-36", "marketing_start_date": "20200821"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (58602-771-40)", "package_ndc": "58602-771-40", "marketing_start_date": "20200821"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (58602-771-41)", "package_ndc": "58602-771-41", "marketing_start_date": "20200821"}, {"sample": false, "description": "600 TABLET in 1 BOTTLE (58602-771-64)", "package_ndc": "58602-771-64", "marketing_start_date": "20210517"}], "brand_name": "Aurophen Extra Strength for Adults", "product_id": "58602-771_0b45ad4e-d9d9-d463-e063-6294a90a195d", "dosage_form": "TABLET", "product_ndc": "58602-771", "generic_name": "Acetaminophen", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aurophen Extra Strength for Adults", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200821", "listing_expiration_date": "20261231"}