Package 50844-175-94

Brand: pain reliever extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50844-175-94
Digits Only 5084417594
Product NDC 50844-175
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-175-94)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0bf1ddc-255d-433a-9810-b22db2e90155", "openfda": {"upc": ["0050844175211"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["8fed703a-9de2-4c76-a783-fcf004f9b890"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-175-12)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-175-12", "marketing_start_date": "19930402"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-175-94)", "package_ndc": "50844-175-94", "marketing_start_date": "19930402"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "50844-175_b0bf1ddc-255d-433a-9810-b22db2e90155", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50844-175", "generic_name": "Acetaminophen", "labeler_name": "L.N.K. International, Inc.", "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"}