VISTASEAL
NDC 61953-0020, Human fibrinogen, human thrombin, solution, from GRIFOLS USA, LLC.
- Product NDC
- 61953-0020
- Status
- Listed
- Labeler
- GRIFOLS USA, LLC
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Product type
- PLASMA DERIVATIVE
- Marketing category
- BLA
- Application
- BLA125640
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/61953-0020 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FIBRINOGEN HUMAN80 mg/mL
- HUMAN THROMBIN500 [iU]/mL
Pharmacologic classes
Blood Coagulation Factors [CS]; Blood Coagulation Factors [CS]; Human Blood Coagulation Factor [EPC]; Human Blood Coagulation Factor [EPC]; Increased Coagulation Activity [PE]; Increased Coagulation Factor Activity [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 61953-0020-1 | 61953002001 | 1 SYRINGE, GLASS in 1 PACKAGE, COMBINATION (61953-0020-1) / 2 mL in 1 SYRINGE, GLASS (61953-0020-2) |
| 61953-0020-3 | 61953002003 | 1 SYRINGE, GLASS in 1 PACKAGE, COMBINATION (61953-0020-3) / 4 mL in 1 SYRINGE, GLASS (61953-0020-4) |
| 61953-0020-5 | 61953002005 | 1 SYRINGE, GLASS in 1 PACKAGE, COMBINATION (61953-0020-5) / 6 mL in 1 SYRINGE, GLASS (61953-0020-6) |
| 61953-0020-7 | 61953002007 | 1 SYRINGE, GLASS in 1 PACKAGE, COMBINATION (61953-0020-7) / 10 mL in 1 SYRINGE, GLASS (61953-0020-8) |
Linked data
RxNorm, label and prices
RxNorm concepts
- 22643712 ML fibrinogen, human 80 MG/ML / thrombin, human 500 UNT/ML Prefilled Syringe [Vistaseal] (SBD)
- 22646044 ML fibrinogen, human 80 MG/ML / thrombin, human 500 UNT/ML Prefilled Syringe [Vistaseal] (SBD)
- 22646076 ML fibrinogen, human 80 MG/ML / thrombin, human 500 UNT/ML Prefilled Syringe [Vistaseal] (SBD)
- 226460910 ML fibrinogen, human 80 MG/ML / thrombin, human 500 UNT/ML Prefilled Syringe [Vistaseal] (SBD)
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 61953-0020 from code or an agent
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Using the healthcare.dev MCP server, look up NDC 61953-0020. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.