Package 79903-342-73

Brand: extra strength pain reliever

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 79903-342-73
Digits Only 7990334273
Product NDC 79903-342
Product ID 79903-342_1e858226-8707-64c7-e063-6294a90a1364
Description

100 TABLET, FILM COATED in 1 BOTTLE (79903-342-73)

Marketing

Marketing Status
Marketed Since 2024-07-30
Brand extra strength pain reliever
Generic acetaminophen
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": "1e858226-8707-64c7-e063-6294a90a1364", "openfda": {"upc": ["0194346263639"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["152bb455-da5b-ae13-e063-6394a90acab0"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (79903-342-73)", "package_ndc": "79903-342-73", "marketing_start_date": "20240730"}], "brand_name": "Extra Strength Pain Reliever", "product_id": "79903-342_1e858226-8707-64c7-e063-6294a90a1364", "dosage_form": "TABLET, FILM COATED", "product_ndc": "79903-342", "generic_name": "Acetaminophen", "labeler_name": "Walmart 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": "20240730", "listing_expiration_date": "20261231"}