NDC 68504-008-01 - PropofolVet Multidose
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
- 68504-008
- Requested NDC
- 68504-008-01
- Package NDCs from labels
- 68504-008-01, 68504-008-02
- Manufacturer
- Parnell Technologies Pty Ltd
- Effective date
- 2025-11-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PropofolVet Multidose - Parnell Technologies Pty Ltd | Parnell Technologies Pty Ltd | 2025-11-26 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68504-008-01 | PropofolVet Multidose | 20 mL in 1 VIAL, MULTI-DOSE | INJECTION, EMULSION | 20 | 2 | |
| 68504-008-01 | PropofolVet Multidose | 5 in 1 CARTON | INJECTION, EMULSION | 5 | 2 |
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.