Package 63323-434-00

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63323-434-00
Digits Only 6332343400
Product NDC 63323-434
Product ID 63323-434_be958bb9-95c1-4525-a145-f1372f08f978
Description

20 BAG in 1 CASE (63323-434-00) / 100 mL in 1 BAG (63323-434-41)

Marketing

Marketing Status
Marketed Since 2020-12-06
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": "be958bb9-95c1-4525-a145-f1372f08f978", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["a0cece43-256e-4adc-92f8-11a0f473bb83"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CASE (63323-434-00)  / 100 mL in 1 BAG (63323-434-41)", "package_ndc": "63323-434-00", "marketing_start_date": "20201206"}], "brand_name": "Acetaminophen", "product_id": "63323-434_be958bb9-95c1-4525-a145-f1372f08f978", "dosage_form": "INJECTION", "product_ndc": "63323-434", "generic_name": "ACETAMINOPHEN", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "NDA204767", "marketing_category": "NDA", "marketing_start_date": "20201206", "listing_expiration_date": "20261231"}