Package 49580-0821-4

Brand: pain relief

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 49580-0821-4
Digits Only 4958008214
Product NDC 49580-0821
Product ID 49580-0821_fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5
Description

1 BOTTLE, PLASTIC in 1 BOX (49580-0821-4) / 118 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2024-07-31
Brand pain relief
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5", "openfda": {"upc": ["0349580281059"], "unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["1c081a7c-8cff-4253-97ac-5fa74a5c0668"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (49580-0821-4)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "49580-0821-4", "marketing_start_date": "20240731"}], "brand_name": "Pain Relief", "product_id": "49580-0821_fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5", "dosage_form": "SUSPENSION", "product_ndc": "49580-0821", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}