# Chlorothiazide

NDC: 63323-658
Generic name: CHLOROTHIAZIDE SODIUM
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20091021

FDA application: ANDA090896

## Active ingredients

- CHLOROTHIAZIDE SODIUM: 500 mg/18mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-658"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-658
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de250776-461a-4d02-a82e-ffedca1a9cf4