Package 63868-679-50

Brand: 8 hour pain relief

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63868-679-50
Digits Only 6386867950
Product NDC 63868-679
Product ID 63868-679_24357a94-9aa7-4606-e063-6294a90ad492
Description

1 BOTTLE, PLASTIC in 1 CARTON (63868-679-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2027-01-31
Brand 8 hour pain relief
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

8 Hour Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24357a94-9aa7-4606-e063-6294a90ad492", "openfda": {"upc": ["0635515958593"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["1da0bd23-9f26-4913-9ebf-1fd8b0fb3bd3"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-679-50)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "63868-679-50", "marketing_end_date": "20270131", "marketing_start_date": "20200801"}], "brand_name": "8 Hour Pain Relief", "product_id": "63868-679_24357a94-9aa7-4606-e063-6294a90ad492", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "63868-679", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "8 Hour Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20200801"}