# Pentamidine Isethionate

NDC: 0121-1101
Generic name: Pentamidine Isethionate
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20260612

FDA application: ANDA206666

## Active ingredients

- PENTAMIDINE DIISETHIONATE: 300 mg/300mg

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-1101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-1101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d46aea4f-8f3f-4ce0-93d6-94e147f5a31a