# Dextrose Monohydrate

NDC: 76329-3302
Generic name: Dextrose Monohydrate
Labeler / Manufacturer: International Medication Systems, Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20211111

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:"76329-3302"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76329-3302
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fcc7ac79-cd70-4f03-a4de-f051f9ca1f7d