# Dexamethasone Sodium Phosphate

NDC: 76045-212
Generic name: DEXAMETHASONE SODIUM PHOSPHATE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20240221

FDA application: ANDA209192

## Active ingredients

- DEXAMETHASONE SODIUM PHOSPHATE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76045-212"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76045-212
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4dd55929-fe0a-4884-ae0d-6f9435920eb7