Package 66715-5680-4

Brand: extra strength pain reliever

Generic: acetaminophen 500 mg, film-coated caplet
NDC Package

Package Facts

Identity

Package NDC 66715-5680-4
Digits Only 6671556804
Product NDC 66715-5680
Product ID 66715-5680_2a838f53-0e3d-3892-e063-6394a90a23d6
Description

1 BOTTLE, PLASTIC in 1 CARTON (66715-5680-4) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2022-05-09
Brand extra strength pain reliever
Generic acetaminophen 500 mg, film-coated caplet
Sample Package No

Linked Drug Pages (1)

Extra Strength Pain Reliever ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a838f53-0e3d-3892-e063-6394a90a23d6", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["e5fd2b46-683e-4cf5-e053-2995a90a5512"], "manufacturer_name": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (66715-5680-4)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "66715-5680-4", "marketing_start_date": "20220509"}], "brand_name": "Extra Strength Pain Reliever", "product_id": "66715-5680_2a838f53-0e3d-3892-e063-6394a90a23d6", "dosage_form": "TABLET, FILM COATED", "product_ndc": "66715-5680", "generic_name": "Acetaminophen 500 mg, film-coated caplet", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220509", "listing_expiration_date": "20261231"}