NDC 73362-102-02 - Yorvipath
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
- 73362-102
- Requested NDC
- 73362-102-02
- Package NDCs from labels
- 73362-102-03, 73362-102-02, 73362-102-01
- Manufacturer
- Ascendis Pharma, Endocrinology, Inc.
- Effective date
- 2026-08-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Yorvipath - Ascendis Pharma, Endocrinology, Inc. | Ascendis Pharma, Endocrinology, Inc. | 2026-08-12 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73362-102-01 | Yorvipath | 2 in 1 CARTON | INJECTION, SOLUTION | 2 | 7 | |
| 73362-102-02 | Yorvipath | 1 in 1 BOX | INJECTION, SOLUTION | 1 | 7 | |
| 73362-102-03 | Yorvipath | 1 in 1 SYRINGE | INJECTION, SOLUTION | 1 | 7 | |
| 73362-102-03 | Yorvipath | 1.4 mL in 1 CARTRIDGE | INJECTION, SOLUTION | 1.4 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 73362-102-01 | ML - Milliliter | 73362-102 | 49fe1412-b591-4d42-8a0f-24c5ce75861b | 1 | 2024-10-04 |
| 73362-102-03 | ML - Milliliter | 73362-102 | 3ee373c0-5147-4af2-90f1-df2d2170be52 | 1 | 2024-10-04 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Yorvipath | PALOPEGTERIPARATIDE | Ascendis Pharma, Endocrinology, Inc. | a1fa23fd-c434-443e-9a17-5750578c8602 | 2026-08-12 | Warnings, Adverse reactions | NDA216490 73362-102-02 73362-100-01 73362-100-03 73362-102-03 73362-100-02 73362-101-01 73362-102-01 73362-101-02 73362-101-03 73362-100 73362-102 73362-101 73362010202 2693637 2693646 2693645 2693647 2693643 2693648 93f0f8d6-548d-4961-bf87-565892563f0e a1fa23fd-c434-443e-9a17-5750578c8602 G2N64C3385 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.