Package 83324-080-01

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 83324-080-01
Digits Only 8332408001
Product NDC 83324-080
Product ID 83324-080_1ac7fa6f-b63f-f915-e063-6294a90a6280
Description

1 BOTTLE, PLASTIC in 1 CARTON (83324-080-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "1ac7fa6f-b63f-f915-e063-6294a90a6280", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["1ac7ed71-5afe-d09c-e063-6294a90a3b88"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-080-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-080-01", "marketing_start_date": "20240403"}], "brand_name": "Pain Relief Extra Strength", "product_id": "83324-080_1ac7fa6f-b63f-f915-e063-6294a90a6280", "dosage_form": "TABLET, COATED", "product_ndc": "83324-080", "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": "20240403", "listing_expiration_date": "20261231"}