NDC 51662-1211

5% DEXTROSE

5% Dextrose

5% DEXTROSE is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Dextrose Monohydrate.

• Product ID: 51662-1211_78817e19-875e-1008-e053-2991aa0ae467
• NDC: 51662-1211
• Product Type: Human Prescription Drug
• Proprietary Name: 5% DEXTROSE
• Generic Name: 5% Dextrose
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2018-10-18
• Marketing Category: NDA / NDA
• Application Number: NDA016367
• Labeler Name: HF Acquisition Co LLC, DBA HealthFirst
• Substance Name: DEXTROSE MONOHYDRATE
• Active Ingredient Strength: 5 g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 51662-1211-1

1 BAG in 1 POUCH (51662-1211-1) > 500 mL in 1 BAG

• Marketing Start Date: 2018-10-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51662-1211-1 [51662121101]

5% DEXTROSE INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA016367
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-10-18
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-02-07

Drug Details

Active Ingredients

Ingredient	Strength
DEXTROSE MONOHYDRATE	5 g/100mL

OpenFDA Data

• SPL SET ID: 78817e19-875d-1008-e053-2991aa0ae467
• Manufacturer:
  • HF Acquisition Co LLC, DBA HealthFirst
• UNII:
  • LX22YL083G
• RxNorm Concept Unique ID - RxCUI:
  • 1795607

NDC Crossover Matching brand name "5% DEXTROSE" or generic name "5% Dextrose"

NDC	Brand Name	Generic Name
51662-1211	5% DEXTROSE	5% DEXTROSE
51662-1413	5% DEXTROSE	5% DEXTROSE