Package 0363-0175-03

Brand: pain reliever extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0363-0175-03
Digits Only 0363017503
Product NDC 0363-0175
Product ID 0363-0175_6434fb16-8cb8-4220-8e85-d9ca1ff51d56
Description

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0175-03)

Marketing

Marketing Status
Marketed Since 1993-04-02
Brand pain reliever extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Reliever Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6434fb16-8cb8-4220-8e85-d9ca1ff51d56", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["f7667529-09c0-4603-8080-f236144fac36"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0175-03)", "package_ndc": "0363-0175-03", "marketing_start_date": "19930402"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "0363-0175_6434fb16-8cb8-4220-8e85-d9ca1ff51d56", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0363-0175", "generic_name": "Acetaminophen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19930402", "listing_expiration_date": "20261231"}