Purple Book product · Reference 351(a)
Campath
alemtuzumab
Oct 12, 2004
Approved
Reference 351(a)
License type
Rx
Marketing
None
Listed patents
Sourced from the FDA Purple Book · verified Jul 02, 2026
Key dates
Approval
Approval date of this BLA submission.
Oct 12, 2004
22 yr 1 mo ago
Orphan exclusivity ends
7-year orphan-drug exclusivity window.
May 07, 2008
18 yr 6 mo ago
Today
Pharmaceutical detail
Strength
30MG/1ML
Dosage form
Injection
Route
Intravenous
Presentation
Single-Dose Vial
Center
CDER
License number
1596
Product number
003
Submission type
Supplement
Supplement number
5034
Change type
Not listed
Reference product family
View full familyThis is the reference (originator) product. Its approved biosimilars and interchangeables are listed below.
1 additional BLA record 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
- v4Jul 02, 2026
- v3Jul 02, 2026
- v2Jul 02, 2026
Frequently asked questions
Does Campath have approved biosimilars?
Yes. 1 approved follow-on biologic reference Campath in the Purple Book: Lemtrada.
What is Campath's BLA number?
Campath is licensed under BLA 103948, held by Genzyme Corporation.
When was Campath approved by the FDA?
Campath was approved by the FDA on Oct 12, 2004.
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.
