Package 79903-268-23

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 79903-268-23
Digits Only 7990326823
Product NDC 79903-268
Product ID 79903-268_543f6901-46aa-4756-9d75-723c13c66cea
Description

225 TABLET in 1 BOTTLE (79903-268-23)

Marketing

Marketing Status
Marketed Since 2024-06-28
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": "543f6901-46aa-4756-9d75-723c13c66cea", "openfda": {"upc": ["0194346266210"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["16d5b56f-7e56-0c91-e063-6394a90a4b8e"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 TABLET in 1 BOTTLE (79903-268-23)", "package_ndc": "79903-268-23", "marketing_start_date": "20240628"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "79903-268_543f6901-46aa-4756-9d75-723c13c66cea", "dosage_form": "TABLET", "product_ndc": "79903-268", "generic_name": "Acetaminophen", "labeler_name": "WALMART INC.", "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": "20240628", "listing_expiration_date": "20261231"}