Package 63868-088-15

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63868-088-15
Digits Only 6386808815
Product NDC 63868-088
Product ID 63868-088_243550ee-8f96-ec2e-e063-6294a90a64f6
Description

150 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-088-15)

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": "243550ee-8f96-ec2e-e063-6294a90a64f6", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["613baf20-00d6-4d44-b18e-8d828a513137"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-088-15)", "package_ndc": "63868-088-15", "marketing_end_date": "20260531", "marketing_start_date": "20120827"}], "brand_name": "Pain Relief Extra Strength", "product_id": "63868-088_243550ee-8f96-ec2e-e063-6294a90a64f6", "dosage_form": "TABLET, COATED", "product_ndc": "63868-088", "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": "20260531", "marketing_start_date": "20120827"}