Package 24201-100-24

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 24201-100-24
Digits Only 2420110024
Product NDC 24201-100
Product ID 24201-100_802892dd-9061-400e-b20d-d7a005b3877f
Description

24 VIAL, GLASS in 1 CARTON (24201-100-24) / 100 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2023-03-01
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "802892dd-9061-400e-b20d-d7a005b3877f", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["b466c989-f7aa-e476-e053-2a95a90a8e55"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 VIAL, GLASS in 1 CARTON (24201-100-24)  / 100 mL in 1 VIAL, GLASS", "package_ndc": "24201-100-24", "marketing_start_date": "20230301"}], "brand_name": "Acetaminophen", "product_id": "24201-100_802892dd-9061-400e-b20d-d7a005b3877f", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "24201-100", "generic_name": "Acetaminophen", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA202605", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}