50% dextrose

Generic: 50% dextrose

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

Drug Facts

Product Profile

Brand Name 50% dextrose
Generic Name 50% 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 51662-1216
Product ID 51662-1216_120092e4-46c1-f9e8-e063-6394a90ae574
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019445
Listing Expiration 2026-12-31
Marketing Start 2018-09-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621216
Hyphenated Format 51662-1216

Supplemental Identifiers

RxCUI
727517
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 50% dextrose (source: ndc)
Generic Name 50% dextrose (source: ndc)
Application Number NDA019445 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 g/50mL
source: ndc
Packaging
  • 1 SYRINGE, PLASTIC in 1 CARTON (51662-1216-1) / 50 mL in 1 SYRINGE, PLASTIC
source: ndc

Packages (1)

51662-1216-1 1 SYRINGE, PLASTIC in 1 CARTON (51662-1216-1) / 50 mL in 1 SYRINGE, PLASTIC

Ingredients (1)

dextrose monohydrate (25 g/50mL)

Linked Drug Pages (1)

50% DEXTROSE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "120092e4-46c1-f9e8-e063-6394a90ae574", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727517"], "spl_set_id": ["763b1cb8-1151-5f59-e053-2991aa0a4e01"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE, PLASTIC in 1 CARTON (51662-1216-1)  / 50 mL in 1 SYRINGE, PLASTIC", "package_ndc": "51662-1216-1", "marketing_start_date": "20180919"}], "brand_name": "50% DEXTROSE", "product_id": "51662-1216_120092e4-46c1-f9e8-e063-6394a90ae574", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1216", "generic_name": "50% DEXTROSE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "50% DEXTROSE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20180919", "listing_expiration_date": "20261231"}