Package 50804-826-03

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50804-826-03
Digits Only 5080482603
Product NDC 50804-826
Product ID 50804-826_24c32d31-dbe9-d726-e063-6394a90a675b
Description

1 BOTTLE, PLASTIC in 1 CARTON (50804-826-03) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2017-08-01
Brand pain relief extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24c32d31-dbe9-d726-e063-6394a90a675b", "openfda": {"upc": ["0846036008265"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["da4339c0-1822-41d8-8c20-214c379a5aa7"], "manufacturer_name": ["GoodSense"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50804-826-03)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50804-826-03", "marketing_start_date": "20170801"}], "brand_name": "Pain Relief Extra Strength", "product_id": "50804-826_24c32d31-dbe9-d726-e063-6394a90a675b", "dosage_form": "TABLET, COATED", "product_ndc": "50804-826", "generic_name": "Acetaminophen", "labeler_name": "GoodSense", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170801", "listing_expiration_date": "20261231"}