Package 70000-0312-1

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 70000-0312-1
Digits Only 7000003121
Product NDC 70000-0312
Description

1 BOTTLE in 1 CARTON (70000-0312-1) / 50 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2004-05-10
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": "2fba5924-6bc0-42d8-84e1-1c581ca2be3a", "openfda": {"upc": ["0096295132335"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["dd8b13a5-07df-4cec-92c3-1a662b1e1a56"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0312-1)  / 50 TABLET, COATED in 1 BOTTLE", "package_ndc": "70000-0312-1", "marketing_start_date": "20040510"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0312-2)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "70000-0312-2", "marketing_start_date": "20040510"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "70000-0312_2fba5924-6bc0-42d8-84e1-1c581ca2be3a", "dosage_form": "TABLET, COATED", "product_ndc": "70000-0312", "generic_name": "Acetaminophen", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "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": "20040510", "listing_expiration_date": "20271231"}