Package 71335-2251-1

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71335-2251-1
Digits Only 7133522511
Product NDC 71335-2251
Description

30 TABLET in 1 BOTTLE (71335-2251-1)

Marketing

Marketing Status
Marketed Since 2024-11-01
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": "8add73d8-1f71-45c6-9ff7-cf71a7ae9029", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["614e69c7-d3cb-4d47-9603-c1c14b87544c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2251-1)", "package_ndc": "71335-2251-1", "marketing_start_date": "20241101"}], "brand_name": "acetaminophen", "product_id": "71335-2251_8add73d8-1f71-45c6-9ff7-cf71a7ae9029", "dosage_form": "TABLET", "product_ndc": "71335-2251", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "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": "20180726", "listing_expiration_date": "20261231"}