Package 69842-931-17

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 69842-931-17
Digits Only 6984293117
Product NDC 69842-931
Description

300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-17)

Marketing

Marketing Status
Marketed Since 2005-12-11
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e241bc2-95ca-4bcf-a1ad-faf575c3d6aa", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["64a1ebe7-af28-4b09-96e8-28fa4dcc52bd"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (69842-931-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "69842-931-08", "marketing_start_date": "20051211"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-17)", "package_ndc": "69842-931-17", "marketing_start_date": "20051211"}, {"sample": false, "description": "150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-29)", "package_ndc": "69842-931-29", "marketing_end_date": "20270131", "marketing_start_date": "20051211"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "69842-931_0e241bc2-95ca-4bcf-a1ad-faf575c3d6aa", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69842-931", "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": "20051211", "listing_expiration_date": "20261231"}