Purple Book product · Reference 351(a)
Novoseven, Novoseven Rt
Coagulation Factor VIIa (Recombinant)
Mar 25, 1999
Approved
Reference 351(a)
License type
Disc
Marketing
None
Listed patents
Sourced from the FDA Purple Book · verified Jul 02, 2026
Key dates
Approval
Approval date of this BLA submission.
Mar 25, 1999
27 yr 9 mo ago
Orphan exclusivity ends
7-year orphan-drug exclusivity window.
Jul 02, 2021
5 yr 1 mo ago
Today
Pharmaceutical detail
Strength
2.4MG
Dosage form
For Injection
Route
Intravenous
Presentation
Single-Dose Vial
Center
CBER
License number
1261
Product number
001
Submission type
Original
Supplement number
0
Change type
Not listed
Reference product family
View full familyThis is the reference (originator) product. No biosimilars or interchangeables reference it in the Purple Book yet.
6 additional BLA records for this product (other strengths or presentations) are in the same reference family.
Patent list
No patent-list records were published for this product. The Purple Book patent list reflects the statutory patent exchange under the BPCIA and is not exhaustive.
Source provenance
- advanced-searchAdvanced Search · Jul 02, 2026
- monthly-downloadMonthly download · Jul 02, 2026
Change history
- v6Jul 02, 2026
- v5Jul 02, 2026
- v4Jul 02, 2026
- v3Jul 02, 2026
- v2Jul 02, 2026
Frequently asked questions
Does Novoseven, Novoseven Rt have approved biosimilars?
No 351(k) biosimilars or interchangeable biosimilars referencing Novoseven, Novoseven Rt are listed in the FDA Purple Book yet.
What is Novoseven, Novoseven Rt's BLA number?
Novoseven, Novoseven Rt is licensed under BLA 103665, held by Novo Nordisk Inc..
When was Novoseven, Novoseven Rt approved by the FDA?
Novoseven, Novoseven Rt was approved by the FDA on Mar 25, 1999.
Related FDA reference tools
- FDA Orange BookApproved drugs, generics, therapeutic-equivalence codes, patents, and exclusivity.
- FDA BiosimilarsThe list of FDA-approved biosimilars and interchangeable biosimilars, by reference product.
- 510(k) Predicate DatabaseSearch FDA 510(k) clearances and map predicate-device lineage.
- FDA 483 & Inspection DatabaseFDA Form 483 observations and inspection records by firm, date, and citation.
