Package 72090-008-01

Brand: acetaminophen 500 mg

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72090-008-01
Digits Only 7209000801
Product NDC 72090-008
Description

500 TABLET in 1 BOTTLE (72090-008-01)

Marketing

Marketing Status
Marketed Since 2024-06-11
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": "5fa2212a-3bf2-43db-aedd-858124e4ed1d", "openfda": {"upc": ["0372090003095"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["0d67bb52-7ae3-439e-9e47-4e21eb0ca352"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72090-008-01)", "package_ndc": "72090-008-01", "marketing_start_date": "20240611"}], "brand_name": "ACETAMINOPHEN 500 MG", "product_id": "72090-008_5fa2212a-3bf2-43db-aedd-858124e4ed1d", "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": "20240611", "listing_expiration_date": "20261231"}