NDC 71872-7329-01 - Auvi-Q
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
- 71872-7329
- Requested NDC
- 71872-7329-01
- Package NDCs from labels
- 71872-7329-1, 71872-7329-01
- Manufacturer
- Medical Purchasing Solutions, LLC
- Effective date
- 2024-12-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Auvi-Q - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2024-12-13 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71872-7329-1 | Auvi-Q | 1 in 1 BAG | INJECTION, SOLUTION | 1 | 1 | |
| 71872-7329-1 | Auvi-Q | 0.3 mL in 1 DOSE PACK | INJECTION, SOLUTION | 0.3 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71872-7329 | AUVI-Q (EPINEPHRINE) INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC] | 1 | Current NDC, 2 package rows | 20241215_29299266-69c5-b1a7-e063-6394a90a25f8.zip |
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 |
|---|---|---|---|---|---|---|
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Baxter Healthcare Corporation | f09f80bf-2f8b-4420-865d-aec2d5e5cd4d | 2012-06-12 | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.