Package 53943-104-02

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 53943-104-02
Digits Only 5394310402
Product NDC 53943-104
Product ID 53943-104_288cbf57-1697-5f70-e063-6394a90af83b
Description

1 BOTTLE, PLASTIC in 1 CARTON (53943-104-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2022-10-01
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": "288cbf57-1697-5f70-e063-6394a90af83b", "openfda": {"upc": ["0093351118890"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["e6fee238-0b6f-cb84-e053-2995a90a361b"], "manufacturer_name": ["DISCOUNT DRUG MART"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (53943-104-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "53943-104-02", "marketing_start_date": "20221001"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (53943-104-04)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "53943-104-04", "marketing_start_date": "20221001"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-104-06)", "package_ndc": "53943-104-06", "marketing_start_date": "20221001"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (53943-104-09)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "53943-104-09", "marketing_start_date": "20221001"}], "brand_name": "Pain Relief Extra Strength", "product_id": "53943-104_288cbf57-1697-5f70-e063-6394a90af83b", "dosage_form": "TABLET, COATED", "product_ndc": "53943-104", "generic_name": "Acetaminophen", "labeler_name": "DISCOUNT DRUG MART", "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": "20221001", "listing_expiration_date": "20261231"}