NDC 0206-3882 - Pipracil
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
- 0206-3882
- Package NDCs from labels
- 0206-3882-55
- Manufacturer
- Wyeth Pharmaceuticals, Inc.
- Effective date
- 2007-04-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PIPRACIL ® (piperacillin for injection) For Intravenous and Intramuscular Use | Wyeth Pharmaceuticals, Inc. | 2007-04-24 | Human prescription drug label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0206-3882-55 | Pipracil | 10 in 1 CARTON | INJECTION, POWDER, LYOPHILIZED, | 10 | 2 | |
| 0206-3882-55 | Pipracil | 1 in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 1 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Piperacillin Sodium | ACTIVE INGREDIENT | M98T69Q7HP | PIPRACIL (PIPERACILLIN SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WYETH PHARMACEUTICALS, INC.] | 2 | |
| Piperacillin | ACTIVE MOIETY | X00B0D5O0E | PIPRACIL (PIPERACILLIN SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [WYETH PHARMACEUTICALS, INC.] | 2 |
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 |
|---|---|---|---|---|---|---|
| 6DF9BFF6-C919-CBB2-24C6-AC873AF37E28 | FAC0C875-111E-4AF2-D186-ED4D4EE9DE59 | 2007-04-24 | Warnings, Adverse reactions | 6DF9BFF6-C919-CBB2-24C6-AC873AF37E28 FAC0C875-111E-4AF2-D186-ED4D4EE9DE59 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.