Package 58602-776-88

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 58602-776-88
Digits Only 5860277688
Product NDC 58602-776
Product ID 58602-776_0b4541a6-ce74-d7e6-e063-6294a90aa709
Description

750 TABLET in 1 BOTTLE (58602-776-88)

Marketing

Marketing Status
Marketed Since 2022-09-02
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0b4541a6-ce74-d7e6-e063-6294a90aa709", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["57bb1acc-b9a0-48cd-8e5c-33712441ce81"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "750 TABLET in 1 BOTTLE (58602-776-88)", "package_ndc": "58602-776-88", "marketing_start_date": "20220902"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "58602-776_0b4541a6-ce74-d7e6-e063-6294a90aa709", "dosage_form": "TABLET", "product_ndc": "58602-776", "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": "20220902", "listing_expiration_date": "20261231"}