United States · FDA National Drug Code directory
Pentamidine Isethionate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0121-1101_f1a6483e-a7cf-4b6e-9372-458a0a8982f9
- Product NDC
- 0121-1101
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Pentamidine Isethionate
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260612
- Source listing expiry
- 20271231
Source-listed ingredients
- PENTAMIDINE DIISETHIONATE — 300 mg/300mg
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-USE in 1 CARTON (0121-1101-02) / 300 mg in 1 VIAL, SINGLE-USE (0121-1101-55) · 0121-1101-02
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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