NDC 71872-7249-01 - Ampicillin
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
- 71872-7249
- Requested NDC
- 71872-7249-01
- Package NDCs from labels
- 71872-7249-1, 71872-7249-01
- Manufacturer
- Medical Purchasing Solutions, LLC
- Effective date
- 2023-04-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ampicillin - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2023-04-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71872-7249-1 | Ampicillin | 1 in 1 BAG | INJECTION, POWDER, FOR SOLUTION | 1 | 2 | |
| 71872-7249-1 | Ampicillin | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71872-7249 | AMPICILLIN INJECTION, POWDER, FOR SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20230429_c4310ee5-cbd3-99b5-e053-2995a90ae229.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 |
|---|---|---|---|---|---|---|
| Ampicillin | AMPICILLIN | Medical Purchasing Solutions, LLC | c4310ee5-cbd3-99b5-e053-2995a90ae229 | 2023-04-27 | Warnings, Adverse reactions | ANDA062772 71872-7249-1 71872-7249 71872724901 1721475 fa59caf4-b361-c99b-e053-6294a90a69e8 c4310ee5-cbd3-99b5-e053-2995a90ae229 JFN36L5S8K |
| Ampicillin | AMPICILLIN SODIUM | Fresenius Kabi USA, LLC | 8dbb4c71-8543-08f1-e053-2995a90af88d | 2022-10-21 | Warnings, Adverse reactions | 1721474 1721475 1721476 1721473 JFN36L5S8K |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.