NDC 0338-8402-01 - TISSEEL Fibrin Sealant
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
- 0338-8402
- Requested NDC
- 0338-8402-01
- Package NDCs from labels
- 0338-8402-01, 0338-8402-02, 0338-8402-03, 0338-8402-04, 0338-8402-09, 0338-8402-10
- Manufacturer
- Baxter Healthcare Corporation
- Effective date
- 2025-09-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TISSEEL Fibrin Sealant - Baxter Healthcare Corporation | Baxter Healthcare Corporation | 2025-09-30 | PLASMA DERIVATIVE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0338-8402-01 | TISSEELFibrin Sealant | 2 mL in 1 SYRINGE, PLASTIC | SOLUTION | 2 | 9 | |
| 0338-8402-02 | TISSEELFibrin Sealant | 1 in 1 CARTON | SOLUTION | 1 | 9 | |
| 0338-8402-03 | TISSEELFibrin Sealant | 4 mL in 1 SYRINGE, PLASTIC | SOLUTION | 4 | 9 | |
| 0338-8402-04 | TISSEELFibrin Sealant | 1 in 1 CARTON | SOLUTION | 1 | 9 | |
| 0338-8402-09 | TISSEELFibrin Sealant | 10 mL in 1 SYRINGE, PLASTIC | SOLUTION | 10 | 9 | |
| 0338-8402-10 | TISSEELFibrin Sealant | 1 in 1 CARTON | SOLUTION | 1 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0338-8402 | TISSEEL FIBRIN SEALANT (FIBRINOGEN HUMAN, HUMAN THROMBIN) KIT TISSEEL FIBRIN SEALANT (FIBRINOGEN HUMAN, HUMAN THROMBIN) SOLUTION [BAXTER HEALTHCARE CORPORATION] | 8 | Legacy NDC, 6 package rows | 20240802_b3f69e25-1b87-4507-81fa-582ea084673d.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0338-8402-01 | ML - Milliliter | 0338-8402 | cbf2520f-e91d-44fa-a468-64bd4e21cbe3 | 1 | 2022-06-06 |
| 0338-8402-02 | ML - Milliliter | 0338-8402 | 95155609-93b5-4cc5-9907-8c99429aef28 | 1 | 2018-01-12 |
| 0338-8402-03 | ML - Milliliter | 0338-8402 | 53cca17c-cdbe-42fb-a3c0-cd18878c3fbe | 1 | 2022-06-06 |
| 0338-8402-04 | ML - Milliliter | 0338-8402 | 18b1ebf7-b9ce-41a9-8593-0bdaefd9efd9 | 1 | 2018-01-12 |
| 0338-8402-09 | ML - Milliliter | 0338-8402 | b6027cf3-c779-4169-8fce-e438b0ba32e6 | 1 | 2022-06-06 |
| 0338-8402-10 | ML - Milliliter | 0338-8402 | ab4c2acb-d2d6-406f-bd13-b1e43ce263ca | 1 | 2018-01-12 |
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 |
|---|---|---|---|---|---|---|
| Protecting base suncream | CITRONELLOL, GERANIOL, LINALOOL | inthismorning co ltd | f3856094-a55a-6982-e053-2a95a90accb2 | 2023-01-30 | Warnings | 25X51I8RD4 |
| Protecting tone up and glow B.B | NIACINAMIDE, ADENOSINE | inthismorning co ltd | f3877ebd-a86a-449b-e053-2995a90a131c | 2023-01-30 | Warnings | 25X51I8RD4 |
| Hydrating all in one concentrate treatment mask | NIACINAMIDE, ADENOSINE | inthismorning co ltd | f3740ff5-2f28-b1bc-e053-2a95a90a6087 | 2023-01-29 | Warnings | 25X51I8RD4 |
| Natrum muriaticum | SODIUM CHLORIDE | Boiron | 86463b98-58f5-7f65-e053-2a91aa0ad3a2 | 2023-01-23 | 451W47IQ8X | |
| Natrum muriaticum | SODIUM CHLORIDE | Boiron | 8645f130-6a19-ae73-e053-2991aa0ab05b | 2023-01-23 | 451W47IQ8X | |
| Natrum muriaticum | SODIUM CHLORIDE | Boiron | 8645eb60-65d1-9d6c-e053-2991aa0a94ef | 2023-01-23 | 451W47IQ8X | |
| Natrum muriaticum | SODIUM CHLORIDE | Boiron | 8644ffef-f0e6-5c06-e053-2a91aa0ae83d | 2023-01-23 | 451W47IQ8X | |
| Natrum muriaticum | SODIUM CHLORIDE | Boiron | 86466614-b8ee-2335-e053-2a91aa0aa67c | 2023-01-23 | 451W47IQ8X | |
| Vitrexyl plus Iron | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | ada43056-a3ce-e7de-e053-2a95a90aa046 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| PureVit DualFe Plus | FERROUS FUMARATE, POLYSACCHARIDE IRON COMPLEX | PureTek Corporation | 71f63741-cad4-43b5-bb3e-c63a188d10a2 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Vitrexyl | FOLIC ACID | PureTek Corporation | ae064a9e-daba-fa86-e053-2a95a90a16a7 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Vitranol Fe | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | b81daf17-430b-6ba2-e053-2a95a90a768b | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Vitrexate | FOLIC ACID | PureTek Corporation | b34fee43-bea9-45b7-e053-2a95a90aad4d | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Vitrexate FE | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | b3637def-a701-673a-e053-2995a90a02d5 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Venexa | FOLIC ACID | PureTek Corporation | ba130779-cdfd-086d-e053-2a95a90a2590 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Venexa FE | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | ba142128-21c4-4204-e053-2a95a90ae0d7 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Ribotin-E | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb1492c5-bfcd-d632-e053-2a95a90ad7d1 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Ventrixyl Fe | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | c7a626ec-88ec-d899-e053-2a95a90ab0ba | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Zintrexyl-C | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb1492c5-bfca-d632-e053-2a95a90ad7d1 | 2023-01-11 | Warnings, Adverse reactions | 25X51I8RD4 |
| Rehydrate | AVENA SATIVA, EQUISETUM HYEMALE, HYPERICUM PERFORATUM, ULMUS FULVA, GLYCYRRHIZA GLABRA, SILICEA, PUERARIA LOBATA, CARLSBAD AQUA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, GERMANIUM SESQUIOXIDE, HYDROGEN, OXYGEN, WIESBADEN | ParaDocs All Natural, Inc. | 648fab10-c46b-420f-a42c-6642009d83fb | 2023-01-10 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.