NDC 67457-351-01 - 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
- 67457-351
- Requested NDC
- 67457-351-01
- Package NDCs from labels
- 67457-351-01, 67457-351-10
- Manufacturer
- Mylan Institutional LLC
- Effective date
- 2018-12-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ampicillin - Mylan Institutional LLC | Mylan Institutional LLC | 2018-12-10 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 67457-351-01 | EA - Each | 67457-351 | fea23bab-5285-4ca7-b93b-86887ed2a2de | 1 | 2017-03-06 |
| 67457-351-10 | EA - Each | 67457-351 | b35957ad-639b-4917-9e3e-f1870474f2d1 | 1 | 2016-10-06 |
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 | JFN36L5S8K |
| Ampicillin | AMPICILLIN SODIUM | Fresenius Kabi USA, LLC | 8dbb4c71-8543-08f1-e053-2995a90af88d | 2022-10-21 | Warnings, Adverse reactions | JFN36L5S8K |
| d5f1a48b-28c5-4264-b2ca-d21f7d105578 | f1ee20ce-df0a-4a30-af90-8ea9577b4814 | 2018-12-10 | Warnings, Adverse reactions | d5f1a48b-28c5-4264-b2ca-d21f7d105578 f1ee20ce-df0a-4a30-af90-8ea9577b4814 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.