Package 81522-070-13

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 81522-070-13
Digits Only 8152207013
Product NDC 81522-070
Product ID 81522-070_1e780586-ce16-1d40-e063-6294a90a79ac
Description

225 TABLET, COATED in 1 BOTTLE, PLASTIC (81522-070-13)

Marketing

Marketing Status
Marketed Since 2024-07-30
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": "1e780586-ce16-1d40-e063-6294a90a79ac", "openfda": {"upc": ["0099581912338"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["1cd6a3e6-1376-0b7b-e063-6394a90af3d1"], "manufacturer_name": ["FSA STORE INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (81522-070-13)", "package_ndc": "81522-070-13", "marketing_start_date": "20240730"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "81522-070_1e780586-ce16-1d40-e063-6294a90a79ac", "dosage_form": "TABLET, COATED", "product_ndc": "81522-070", "generic_name": "Acetaminophen", "labeler_name": "FSA STORE INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240730", "listing_expiration_date": "20261231"}