NDC 63323-321-01 - POLYMYXIN B
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
- 63323-321
- Requested NDC
- 63323-321-01
- Package NDCs from labels
- 63323-321-02, 63323-321-12, 63323-321-01, 63323-321-10
- Manufacturer
- Fresenius Kabi USA, LLC
- Effective date
- 2021-05-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| POLYMYXIN B - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2021-05-31 | HUMAN PRESCRIPTION DRUG LABEL |
| POLYMYXIN B - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2021-02-28 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63323-321-01 | POLYMYXIN B | 1 in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 1 | 4 | |
| 63323-321-10 | POLYMYXIN B | 10 in 1 TRAY | INJECTION, POWDER, LYOPHILIZED, | 10 | 4 | |
| 63323-321-02 | POLYMYXIN B | 1 in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 1 | 1 | |
| 63323-321-12 | POLYMYXIN B | 10 in 1 TRAY | INJECTION, POWDER, LYOPHILIZED, | 10 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63323-321 | POLYMYXIN B (POLYMYXIN B SULFATE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC ] | 4 | Current NDC, Legacy NDC, 2 package rows | 20210319_fbc12c18-567b-41bc-89d0-efd29616615c.zip |
| 63323-321 | POLYMYXIN B (POLYMYXIN B SULFATE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC ] | 1 | Current NDC, Legacy NDC, 2 package rows | 20210610_704a41f5-b109-4c16-8d3e-1495c9917952.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63323-321-01 | EA - Each | 63323-321 | be16a189-5df5-47a8-b45a-cdb1b65a94c3 | 1 | 2021-12-08 |
| 63323-321-02 | EA - Each | 63323-321 | bfda5fd4-1a9f-4670-9011-10eec3ecb30f | 1 | 2021-12-08 |
| 63323-321-10 | EA - Each | 63323-321 | 39fc3b1f-87de-48e0-876a-de660dbc6b0b | 1 | 2012-07-24 |
| 63323-321-12 | EA - Each | 63323-321 | b3ba8ab7-008d-430e-a375-60326f0daeb8 | 1 | 2021-12-08 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| POLYMYXIN B SULFATE | ACTIVE INGREDIENT | 19371312D4 | POLYMYXIN B (POLYMYXIN B SULFATE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC] | 2 | |
| POLYMYXIN B | ACTIVE MOIETY | J2VZ07J96K | POLYMYXIN B (POLYMYXIN B SULFATE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC] | 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 |
|---|---|---|---|---|---|---|
| Trimethoprim sulfate and Polymyxin B sulfate | TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE | Proficient Rx LP | 2c5579eb-ad81-415e-8dcb-9f1c94c897ae | 2021-01-01 | Warnings, Adverse reactions | 19371312D4 |
| Neomycin and Polymyxin B Sulfates and Hydrocortisone | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE | Proficient Rx LP | d55f1783-9c49-4f90-9ff8-6f132e7b325e | 2021-01-01 | Boxed warning, Warnings, Adverse reactions | 19371312D4 |
| Neomycin and Polymyxin B Sulfates and Dexamethasone | NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE | Proficient Rx LP | aa7b8a3f-06dd-4190-96a5-f86195bd2197 | 2021-01-01 | Warnings, Adverse reactions | 19371312D4 |
| Neomycin and Polymyxin B Sulfates and Hydrocortisone | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE | Asclemed USA, Inc. | 7c78ec84-8b7c-42f1-a879-3bf27a1daa71 | 2020-10-30 | Boxed warning, Warnings, Adverse reactions | 19371312D4 |
| Water-Jel 3-in-1 Antibiotic | BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE | Water-Jel Technologies | d5fcaffd-af38-4285-a79c-6df7424c76fa | 2017-11-16 | Warnings | 19371312D4 |
| CVS Triple Antibiotic | BACITRACIN, NEOMYCIN, POLYMYXIN B | CVS Pharmacy | 454bfeed-f58f-003a-e054-00144ff8d46c | 2017-01-04 | Warnings | 19371312D4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.