Package 63868-507-01

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63868-507-01
Digits Only 6386850701
Product NDC 63868-507
Product ID 63868-507_243562aa-4855-9d50-e063-6394a90a7cac
Description

1 BOTTLE, PLASTIC in 1 CARTON (63868-507-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-12-31
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": "243562aa-4855-9d50-e063-6394a90a7cac", "openfda": {"upc": ["0635515957718"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["5de40821-3218-4320-bf11-9493bf01d489"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-507-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-507-01", "marketing_end_date": "20261231", "marketing_start_date": "20070814"}], "brand_name": "Pain Relief Extra Strength", "product_id": "63868-507_243562aa-4855-9d50-e063-6394a90a7cac", "dosage_form": "TABLET, COATED", "product_ndc": "63868-507", "generic_name": "Acetaminophen", "labeler_name": "Chain Drug Marketing Association", "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": "20261231", "marketing_start_date": "20070814"}