Package 41415-538-10

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 41415-538-10
Digits Only 4141553810
Product NDC 41415-538
Description

100 TABLET in 1 BOTTLE (41415-538-10)

Marketing

Marketing Status
Marketed Since 2024-09-09
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46a1f171-7946-2ec6-e063-6394a90a60e2", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["08f5af1d-365b-a97c-e063-6394a90a99ae"], "manufacturer_name": ["PUBLIX SUPERMARKETS, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (41415-538-05)", "package_ndc": "41415-538-05", "marketing_start_date": "20240909"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (41415-538-10)", "package_ndc": "41415-538-10", "marketing_start_date": "20240909"}], "brand_name": "Acetaminophen", "product_id": "41415-538_46a1f171-7946-2ec6-e063-6394a90a60e2", "dosage_form": "TABLET", "product_ndc": "41415-538", "generic_name": "Acetaminophen", "labeler_name": "PUBLIX SUPERMARKETS, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240909", "listing_expiration_date": "20261231"}