Package 50844-951-20

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50844-951-20
Digits Only 5084495120
Product NDC 50844-951
Product ID 50844-951_30ddbaa9-9ef6-41d9-b257-ae3003113729
Description

225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-951-20)

Marketing

Marketing Status
Discontinued 2026-05-31
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": "30ddbaa9-9ef6-41d9-b257-ae3003113729", "openfda": {"upc": ["0350844951205"], "unii": ["362O9ITL9D"], "spl_set_id": ["09c9a9d9-f14e-4343-9677-188f20d4d148"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-951-15)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-951-15", "marketing_end_date": "20260531", "marketing_start_date": "20040510"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-951-20)", "package_ndc": "50844-951-20", "marketing_end_date": "20260531", "marketing_start_date": "20040510"}], "brand_name": "Pain Relief Extra Strength", "product_id": "50844-951_30ddbaa9-9ef6-41d9-b257-ae3003113729", "dosage_form": "TABLET, COATED", "product_ndc": "50844-951", "generic_name": "Acetaminophen", "labeler_name": "L.N.K. International, Inc.", "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_end_date": "20260531", "marketing_start_date": "20040510"}