Package 70518-4184-2

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 70518-4184-2
Digits Only 7051841842
Product NDC 70518-4184
Product ID 70518-4184_3ff14a1e-fe75-90c9-e063-6294a90a7e24
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4184-2) / 100 mL in 1 VIAL, SINGLE-DOSE (70518-4184-3)

Marketing

Marketing Status
Marketed Since 2024-09-30
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": "3ff14a1e-fe75-90c9-e063-6294a90a7e24", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["464e404a-1957-44a2-a53a-f2a9d3c15bde"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4184-2)  / 100 mL in 1 VIAL, SINGLE-DOSE (70518-4184-3)", "package_ndc": "70518-4184-2", "marketing_start_date": "20240930"}], "brand_name": "Acetaminophen", "product_id": "70518-4184_3ff14a1e-fe75-90c9-e063-6294a90a7e24", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "70518-4184", "generic_name": "Acetaminophen", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA210969", "marketing_category": "ANDA", "marketing_start_date": "20240924", "listing_expiration_date": "20261231"}