NDC product
Pentamidine Isethionate
NDC 0121-1101 · PAI Holdings, LLC dba PAI Pharma
Key facts
| Product NDC | 0121-1101 |
|---|---|
| Proprietary name | Pentamidine Isethionate |
| Nonproprietary name | Pentamidine Isethionate |
| Substances | PENTAMIDINE DIISETHIONATE |
| Dosage form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAMUSCULAR, INTRAVENOUS |
| Labeler | PAI Holdings, LLC dba PAI Pharma |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA206666 |
| Pharmacologic classes | Antiprotozoal [EPC] |
| Marketing start | Jun 12, 2026 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: