Package 54257-573-03

Brand: acetaminophen extended-release

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 54257-573-03
Digits Only 5425757303
Product NDC 54257-573
Description

200 TABLET in 1 BOTTLE (54257-573-03)

Marketing

Marketing Status
Marketed Since 2020-01-24
Brand acetaminophen extended-release
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf6e6c2c-3775-f475-e053-2995a90a2754", "openfda": {"upc": ["0043292565239"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["9d22bedb-9fc9-8421-e053-2a95a90acf4a"], "manufacturer_name": ["Magno-Humphries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (54257-573-03)", "package_ndc": "54257-573-03", "marketing_start_date": "20200124"}], "brand_name": "Acetaminophen Extended-Release", "product_id": "54257-573_cf6e6c2c-3775-f475-e053-2995a90a2754", "dosage_form": "TABLET", "product_ndc": "54257-573", "generic_name": "ACETAMINOPHEN", "labeler_name": "Magno-Humphries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Extended-Release", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20200124", "listing_expiration_date": "20261231"}