# Dextrose and Sodium Chloride

NDC: 0338-0077
Generic name: Dextrose and Sodium Chloride
Labeler / Manufacturer: Baxter Healthcare Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 19701208

FDA application: NDA016689

## Active ingredients

- DEXTROSE MONOHYDRATE: 5 g/100mL
- SODIUM CHLORIDE: 200 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0077"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0077
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dcbf1907-1841-4afc-ab5d-a9893a2d7256