Package 51662-1215-1

Brand: dextrose

Generic: dextrose
NDC Package

Package Facts

Identity

Package NDC 51662-1215-1
Digits Only 5166212151
Product NDC 51662-1215
Product ID 51662-1215_11c3db4a-10d2-24e8-e063-6294a90a4167
Description

50 mL in 1 VIAL, SINGLE-DOSE (51662-1215-1)

Marketing

Marketing Status
Marketed Since 2018-09-13
Brand dextrose
Generic dextrose
Sample Package No

Linked Drug Pages (1)

DEXTROSE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "11c3db4a-10d2-24e8-e063-6294a90a4167", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["1795514"], "spl_set_id": ["75c902e8-50e7-a337-e053-2991aa0a2093"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, SINGLE-DOSE (51662-1215-1)", "package_ndc": "51662-1215-1", "marketing_start_date": "20180913"}], "brand_name": "DEXTROSE", "product_id": "51662-1215_11c3db4a-10d2-24e8-e063-6294a90a4167", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1215", "generic_name": "DEXTROSE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20180913", "listing_expiration_date": "20261231"}