# Dextrose monohydrate

NDC: 51662-1584
Generic name: Dextrose monohydrate
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220211

FDA application: ANDA203451

## Active ingredients

- DEXTROSE MONOHYDRATE: 25 g/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1584"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1584
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7c4f9eb-9b89-c5a3-e053-2a95a90a28a2