Package 72162-2179-1

Brand: extra strength acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72162-2179-1
Digits Only 7216221791
Product NDC 72162-2179
Product ID 72162-2179_0148ca05-29b7-4155-8403-28dfbe09fc20
Description

100 TABLET in 1 BOTTLE (72162-2179-1)

Marketing

Marketing Status
Marketed Since 2024-02-02
Brand extra strength acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Extra Strength Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0148ca05-29b7-4155-8403-28dfbe09fc20", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ea417ddb-54b3-49e2-bec1-8fe450d9990c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2179-1)", "package_ndc": "72162-2179-1", "marketing_start_date": "20240202"}], "brand_name": "Extra Strength Acetaminophen", "product_id": "72162-2179_0148ca05-29b7-4155-8403-28dfbe09fc20", "dosage_form": "TABLET", "product_ndc": "72162-2179", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180701", "listing_expiration_date": "20261231"}