Package 51662-1453-1

Brand: dextrose monohydrate

Generic: dextrose monohydrate
NDC Package

Package Facts

Identity

Package NDC 51662-1453-1
Digits Only 5166214531
Product NDC 51662-1453
Description

1 SYRINGE in 1 CARTON (51662-1453-1) / 50 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2020-01-11
Brand dextrose monohydrate
Generic dextrose monohydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ef7c1a32-f72c-3c5a-e053-2995a90abd43", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727517"], "spl_set_id": ["9bd8168d-ab8f-4d70-e053-2995a90ac23c"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (51662-1453-1)  / 50 mL in 1 SYRINGE", "package_ndc": "51662-1453-1", "marketing_start_date": "20200111"}], "brand_name": "DEXTROSE MONOHYDRATE", "product_id": "51662-1453_ef7c1a32-f72c-3c5a-e053-2995a90abd43", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1453", "generic_name": "DEXTROSE MONOHYDRATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE MONOHYDRATE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200111", "listing_expiration_date": "20261231"}