Package 49580-2880-4

Brand: pain reliever

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 49580-2880-4
Digits Only 4958028804
Product NDC 49580-2880
Product ID 49580-2880_7dfcadc9-97a1-4d12-b8d9-2053c4ee9273
Description

1 BOTTLE, PLASTIC in 1 BOX (49580-2880-4) / 118 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-12-30
Brand pain reliever
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Reliever ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7dfcadc9-97a1-4d12-b8d9-2053c4ee9273", "openfda": {"upc": ["0349580288058"], "unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["64c642b7-ef83-44b7-a014-6fa248dff3ba"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (49580-2880-4)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "49580-2880-4", "marketing_end_date": "20261230", "marketing_start_date": "20240315"}], "brand_name": "Pain Reliever", "product_id": "49580-2880_7dfcadc9-97a1-4d12-b8d9-2053c4ee9273", "dosage_form": "SUSPENSION", "product_ndc": "49580-2880", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261230", "marketing_start_date": "20240315"}