NDC 63323-596-06 - Glucagon
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
- 63323-596
- Requested NDC
- 63323-596-06
- Package NDCs from labels
- 63323-596-08, 63323-596-16, 63323-596-06, 63323-596-11, 63323-596-13, 63323-596-03
- Manufacturer
- Fresenius Kabi USA, LLC
- Effective date
- 2022-04-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Glucagon - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Glucagon - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2020-09-16 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63323-596-11 | Glucagon | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION, POWDER, LYOPHILIZED, | 1 | 7 | |
| 63323-596-13 | Glucagon | 10 in 1 TRAY | INJECTION, POWDER, LYOPHILIZED, | 10 | 7 | |
| 63323-596-08 | Glucagon | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION, POWDER, LYOPHILIZED, | 1 | 6 | |
| 63323-596-16 | Glucagon | 10 in 1 TRAY | INJECTION, POWDER, LYOPHILIZED, | 10 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63323-596 | GLUCAGON INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION GLUCAGON KIT [FRESENIUS KABI USA, LLC] | 7 | Current NDC, Legacy NDC, 2 package rows | 20211118_e4be1c0e-0fe6-45a0-9229-5cde98434b84.zip |
| 63323-596 | GLUCAGON INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION GLUCAGON KIT [FRESENIUS KABI USA, LLC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20220420_8c8acad6-44cc-43aa-966b-027e053be8f5.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63323-596-08 | EA - Each | 63323-596 | fe2f13d2-b25a-41e9-8f9e-0bb3462b9d68 | 1 | 2022-10-06 |
| 63323-596-11 | EA - Each | 63323-596 | 037fd4b8-d779-4b81-9b86-3e6be92e4578 | 1 | 2023-03-13 |
| 63323-596-13 | EA - Each | 63323-596 | eb692baf-7a37-49d4-83dc-af1f928cbe4d | 1 | 2015-06-09 |
| 63323-596-16 | EA - Each | 63323-596 | 5cb3c2fe-c644-4772-975f-ef574abc9f1e | 1 | 2015-12-02 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Bio Rock Water | ROCK WATER | BioActive Nutritional, Inc. | 178bd16d-0d4f-49d8-866b-8ab3a3c6889d | 2018-07-30 | Warnings | 059QF0KO0R |
| 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.