Package 0363-0892-04

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0363-0892-04
Digits Only 0363089204
Product NDC 0363-0892
Description

20 TABLET in 1 BOTTLE (0363-0892-04)

Marketing

Marketing Status
Marketed Since 2024-07-23
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": "46549261-e3e0-1689-e063-6394a90acda3", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["0944a5d4-2ccc-5f0d-e063-6394a90a8af9"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (0363-0892-04)", "package_ndc": "0363-0892-04", "marketing_start_date": "20240723"}], "brand_name": "Acetaminophen", "product_id": "0363-0892_46549261-e3e0-1689-e063-6394a90acda3", "dosage_form": "TABLET", "product_ndc": "0363-0892", "generic_name": "Acetaminophen", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20240723", "listing_expiration_date": "20261231"}