dextrose

Generic: dextrose

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose
Generic Name dextrose
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 25 g/50mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1215
Product ID 51662-1215_11c3db4a-10d2-24e8-e063-6294a90a4167
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019445
Listing Expiration 2026-12-31
Marketing Start 2018-09-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621215
Hyphenated Format 51662-1215

Supplemental Identifiers

RxCUI
1795514
UNII
LX22YL083G

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dextrose (source: ndc)
Generic Name dextrose (source: ndc)
Application Number NDA019445 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 g/50mL
source: ndc
Packaging
  • 50 mL in 1 VIAL, SINGLE-DOSE (51662-1215-1)
source: ndc

Packages (1)

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

Ingredients (1)

dextrose monohydrate (25 g/50mL)

Linked Drug Pages (1)

DEXTROSE ndc-match (0.9)

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"}