Package 50844-255-08

Brand: pain reliever

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50844-255-08
Digits Only 5084425508
Product NDC 50844-255
Description

1 BOTTLE, PLASTIC in 1 CARTON (50844-255-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2019-07-23
Brand pain reliever
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cb980327-4973-491f-904d-1193ef3a51ec", "openfda": {"upc": ["0052548689902"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["734cc3d2-6fc5-4dcc-93ed-0b57c1f01345"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-255-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-255-08", "marketing_start_date": "20190723"}], "brand_name": "Pain Reliever", "product_id": "50844-255_cb980327-4973-491f-904d-1193ef3a51ec", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50844-255", "generic_name": "Acetaminophen", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190723", "listing_expiration_date": "20261231"}