NDC 72485-417-01 - Ampicillin Sodium and Sulbactam Sodium
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
- 72485-417
- Requested NDC
- 72485-417-01
- Package NDCs from labels
- 72485-417-01, 72485-417-10
- Manufacturer
- Armas Pharmaceuticals Inc. | Onesource Specialty Pte. Limited | Onesource Specialty Private Limited - Beta Lactam Division
- Effective date
- 2025-07-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ampicillin and Sulbactam for Injection, USP | Armas Pharmaceuticals Inc. | Onesource Specialty Pte. Limited | Onesource Specialty Private Limited - Beta Lactam Division | 2025-07-31 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72485-417-01 | Ampicillin Sodium and Sulbactam Sodium | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | 4 | |
| 72485-417-10 | Ampicillin Sodium and Sulbactam Sodium | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72485-417 | AMPICILLIN SODIUM AND SULBACTAM SODIUM (AMPICILLIN SODIUM, SULBACTAM SODIUM) INJECTION, POWDER, FOR SOLUTION [ARMAS PHARMACEUTICALS INC.] | 3 | Current NDC, 2 package rows | 20241030_ac6f8158-9d7e-4b99-af3c-0407c5287b57.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72485-417-01 | EA - Each | 72485-417 | 89b4dbb5-4a30-4320-97b7-e2ed45a223c5 | 1 | 2023-05-05 |
| 72485-417-10 | EA - Each | 72485-417 | 1d805698-bd09-42f2-b7a7-31a3a31fc886 | 1 | 2023-05-05 |
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 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.