Package 72090-008-30

Brand: acetaminophen 500 mg

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72090-008-30
Digits Only 7209000830
Product NDC 72090-008
Description

300 TABLET in 1 BOTTLE (72090-008-30)

Marketing

Marketing Status
Marketed Since 2023-05-11
Brand acetaminophen 500 mg
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c7221f1d-d823-4514-a3a8-8d02afbb43fd", "openfda": {"upc": ["0372090000490"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["11e6ec2a-5171-4496-a15f-6ff744bd1f2f"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (72090-008-30)", "package_ndc": "72090-008-30", "marketing_start_date": "20230511"}], "brand_name": "ACETAMINOPHEN 500 MG", "product_id": "72090-008_c7221f1d-d823-4514-a3a8-8d02afbb43fd", "dosage_form": "TABLET", "product_ndc": "72090-008", "generic_name": "ACETAMINOPHEN", "labeler_name": "Pioneer Life Sciences, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN 500 MG", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230511", "listing_expiration_date": "20261231"}