Package 68998-004-06

Brand: pain reliever extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 68998-004-06
Digits Only 6899800406
Product NDC 68998-004
Product ID 68998-004_28735d9d-6830-a776-e063-6394a90a9b8d
Description

500 TABLET, COATED in 1 BOTTLE, PLASTIC (68998-004-06)

Marketing

Marketing Status
Discontinued 2027-03-31
Brand pain reliever extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Reliever Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "28735d9d-6830-a776-e063-6394a90a9b8d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["43bf297f-2832-424f-a013-4bfa1d6c03e6"], "manufacturer_name": ["Marc Glassman, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (68998-004-06)", "package_ndc": "68998-004-06", "marketing_end_date": "20270331", "marketing_start_date": "20080301"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "68998-004_28735d9d-6830-a776-e063-6394a90a9b8d", "dosage_form": "TABLET, COATED", "product_ndc": "68998-004", "generic_name": "Acetaminophen", "labeler_name": "Marc Glassman, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270331", "marketing_start_date": "20080301"}