Package 55150-307-24

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 55150-307-24
Digits Only 5515030724
Product NDC 55150-307
Product ID 55150-307_ddbd820d-6245-44a7-b539-3c6813ffa58a
Description

24 VIAL, SINGLE-DOSE in 1 CARTON (55150-307-24) / 100 mL in 1 VIAL, SINGLE-DOSE (55150-307-01)

Marketing

Marketing Status
Marketed Since 2020-10-21
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": "ddbd820d-6245-44a7-b539-3c6813ffa58a", "openfda": {"upc": ["0355150307012"], "unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["f80b6f72-f280-4b4a-a6a9-e6490b94705b"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 VIAL, SINGLE-DOSE in 1 CARTON (55150-307-24)  / 100 mL in 1 VIAL, SINGLE-DOSE (55150-307-01)", "package_ndc": "55150-307-24", "marketing_start_date": "20201021"}], "brand_name": "Acetaminophen", "product_id": "55150-307_ddbd820d-6245-44a7-b539-3c6813ffa58a", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "55150-307", "generic_name": "Acetaminophen", "labeler_name": "Eugia US LLC", "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": "20201021", "listing_expiration_date": "20261231"}