Package 63868-084-05

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63868-084-05
Digits Only 6386808405
Product NDC 63868-084
Description

500 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-084-05)

Marketing

Marketing Status
Marketed Since 2014-06-13
Brand pain relief 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": "243531d9-3c42-d20a-e063-6294a90a2b09", "openfda": {"upc": ["0635515908420"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["68a52858-35c5-402a-8ceb-8d8a7c1e5f6c"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-084-05)", "package_ndc": "63868-084-05", "marketing_start_date": "20140613"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-084-10)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-084-10", "marketing_end_date": "20260831", "marketing_start_date": "20140613"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-084-24)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-084-24", "marketing_end_date": "20260831", "marketing_start_date": "20140613"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-084-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-084-50", "marketing_end_date": "20260831", "marketing_start_date": "20140613"}], "brand_name": "Pain Relief Extra Strength", "product_id": "63868-084_243531d9-3c42-d20a-e063-6294a90a2b09", "dosage_form": "TABLET, COATED", "product_ndc": "63868-084", "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_start_date": "20140613", "listing_expiration_date": "20261231"}