Package 63941-303-04

Brand: extra strength pain relief

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63941-303-04
Digits Only 6394130304
Product NDC 63941-303
Product ID 63941-303_45b2da7e-84d3-5b1d-e063-6394a90a0cf8
Description

1 BOTTLE, PLASTIC in 1 CARTON (63941-303-04) / 100 TABLET in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2027-09-30
Brand extra strength pain relief
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Extra Strength Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45b2da7e-84d3-5b1d-e063-6394a90a0cf8", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["5a80cb17-7731-4457-acd3-64cf4accf862"], "manufacturer_name": ["VALU MERCHANDISERS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-303-04)  / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "63941-303-04", "marketing_end_date": "20270930", "marketing_start_date": "20091125"}], "brand_name": "Extra Strength Pain Relief", "product_id": "63941-303_45b2da7e-84d3-5b1d-e063-6394a90a0cf8", "dosage_form": "TABLET", "product_ndc": "63941-303", "generic_name": "Acetaminophen", "labeler_name": "VALU MERCHANDISERS COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270930", "marketing_start_date": "20091125"}