FDA NDC Directory · JSON-LD · Markdown
NDC 43598-649 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Labeler / Manufacturer | Dr.Reddy's Laboratories Inc., |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA210214 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS |
| Active ingredients | TREPROSTINIL (20 mg/20mL) |
| Marketing started | 20230213 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).