NDC 0641-6166-01 - Amikacin Sulfate
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
- 0641-6166
- Requested NDC
- 0641-6166-01
- Package NDCs from labels
- 0641-6166-01, 0641-6166-10
- Manufacturer
- Hikma Pharmaceuticals USA Inc.
- Effective date
- 2024-04-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AMIKACIN SULFATE INJECTION, USP | Hikma Pharmaceuticals USA Inc. | 2024-04-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0641-6166-01 | Amikacin Sulfate | 4 mL in 1 VIAL | INJECTION | 4 | 10 | |
| 0641-6166-10 | Amikacin Sulfate | 10 in 1 CARTON | INJECTION | 10 | 10 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0641-6166-01 | ML - Milliliter | 0641-6166 | 3cfe97bf-23bc-48b5-82f2-8afece928a16 | 1 | 2016-01-13 |
| 0641-6166-10 | ML - Milliliter | 0641-6166 | 3b98a712-a6ff-48bd-bc4f-95d6ae0cc65a | 1 | 2016-01-13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| AMIKACIN SULFATE | ACTIVE INGREDIENT | N6M33094FD | AMIKACIN SULFATE INJECTION [WEST-WARD PHARMACEUTICALS CORP.] | 3 | |
| AMIKACIN | ACTIVE MOIETY | 84319SGC3C | AMIKACIN SULFATE INJECTION [WEST-WARD PHARMACEUTICALS CORP.] | 3 | |
| SODIUM CITRATE, UNSPECIFIED FORM | INACTIVE INGREDIENT | 1Q73Q2JULR | AMIKACIN SULFATE INJECTION [WEST-WARD PHARMACEUTICALS CORP.] | 3 | |
| SODIUM METABISULFITE | INACTIVE INGREDIENT | 4VON5FNS3C | AMIKACIN SULFATE INJECTION [WEST-WARD PHARMACEUTICALS CORP.] | 3 | |
| SULFURIC ACID | INACTIVE INGREDIENT | O40UQP6WCF | AMIKACIN SULFATE INJECTION [WEST-WARD PHARMACEUTICALS CORP.] | 3 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | AMIKACIN SULFATE INJECTION [WEST-WARD PHARMACEUTICALS CORP.] | 3 |
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 |
|---|---|---|---|---|---|---|
| Trauma plus Gel | CALENDULA OFFICINALIS, ARNICA MONTANA, HYPERICUM PERFORATUM, SYMPHYTUM OFFICINALE, BELLIS PERENNIS, LEDUM PALUSTRE, SULPHURICUM ACIDUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, RHUS TOX, RUTA GRAVEOLENS, NATRUM SULPHURICUM | Energique, Inc. | 6da04ff9-4088-427c-9757-36092c8f7585 | 2018-02-08 | Warnings | O40UQP6WCF |
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.