Package 11673-105-26

Brand: up and up childrens acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 11673-105-26
Digits Only 1167310526
Product NDC 11673-105
Product ID 11673-105_9bc7510c-d284-4ca5-8a86-a346f690f3b1
Description

1 BOTTLE in 1 CARTON (11673-105-26) / 118 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2009-07-08
Brand up and up childrens acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Up and Up childrens acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9bc7510c-d284-4ca5-8a86-a346f690f3b1", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["9c3ba4dd-f51b-46ce-91b8-8b617c7b78da"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-105-26)  / 118 mL in 1 BOTTLE", "package_ndc": "11673-105-26", "marketing_start_date": "20090708"}], "brand_name": "Up and Up childrens acetaminophen", "product_id": "11673-105_9bc7510c-d284-4ca5-8a86-a346f690f3b1", "dosage_form": "SUSPENSION", "product_ndc": "11673-105", "generic_name": "Acetaminophen", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up childrens acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090708", "listing_expiration_date": "20261231"}