Package 69842-750-03

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 69842-750-03
Digits Only 6984275003
Product NDC 69842-750
Product ID 69842-750_dddce8af-b0ec-402c-ae95-a548ad915d23
Description

1 BOTTLE in 1 PACKAGE (69842-750-03) / 10 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 1993-04-02
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dddce8af-b0ec-402c-ae95-a548ad915d23", "openfda": {"upc": ["0050428089507"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["afacdc0b-fb65-464e-91b8-e82ba7ecde44"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 PACKAGE (69842-750-03)  / 10 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-750-03", "marketing_start_date": "19930402"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "69842-750_dddce8af-b0ec-402c-ae95-a548ad915d23", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69842-750", "generic_name": "Acetaminophen", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19930402", "listing_expiration_date": "20261231"}