NDC 72603-201 - Leuprolide Acetate
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 72603-201
- Package NDCs from labels
- 72603-201-01
- Manufacturer
- NorthStar RxLLC | RK Pharma INC
- Effective date
- 2025-06-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Leuprolide Acetate - NorthStar RxLLC | RK Pharma INC | NorthStar RxLLC | RK Pharma INC | 2025-06-24 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72603-201-01 | Leuprolide Acetate | 2.8 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 2.8 mL | 5 mg in 1mL | 7 |
| 72603-201-01 | Leuprolide Acetate | 1 in 1 CARTON | INJECTION, SOLUTION | 5 mg in 1mL | 7 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.