# Dexamethasone Sodium Phosphate

NDC: 81565-202
Generic name: DEXAMETHASONE SODIUM PHOSPHATE
Labeler / Manufacturer: Phlow Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20211215

FDA application: ANDA084916

## Active ingredients

- DEXAMETHASONE SODIUM PHOSPHATE: 4 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81565-202"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81565-202
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02d25ab8-8f51-452b-b944-f569fbae36fe