Package 83324-079-50

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 83324-079-50
Digits Only 8332407950
Product NDC 83324-079
Product ID 83324-079_1ac6f38b-c82f-7621-e063-6394a90aae83
Description

1 BOTTLE, PLASTIC in 1 CARTON (83324-079-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2024-04-29
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": "1ac6f38b-c82f-7621-e063-6394a90aae83", "openfda": {"upc": ["0635515957350"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["9fdbaf5e-f88b-4d18-97df-0b2e8dddf377"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-079-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-079-50", "marketing_start_date": "20240429"}], "brand_name": "Pain Relief Extra Strength", "product_id": "83324-079_1ac6f38b-c82f-7621-e063-6394a90aae83", "dosage_form": "TABLET, COATED", "product_ndc": "83324-079", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC.", "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": "20240429", "listing_expiration_date": "20261231"}