dalbavancin hydrochloride · Abbvie · NDA 021883
Dalvance
Earliest generic entry, as listed
23 May 2028
Blocked by patent: US 6900175. Only method-of-use patents remain, so a generic may carve out the protected indication and enter earlier.
Listed patents · 1 unexpired
| Patent | Claims | Expires |
|---|---|---|
| US 6900175 | use U-3499 | 23 May 2028 |
Exclusivities · 0 unexpired
No unexpired exclusivities listed.
Paragraph IV certifications · 0
No Paragraph IV certification listed by FDA for this drug.
The list shows that a generic applicant certified to FDA that a listed patent is invalid or not infringed. It does not show litigation, settlements or launch timing.
Event history
- 25 Oct 2026First generic approved · 021883-00123 Oct 2025
- 25 Oct 2026Generic approved · 021883-00123 Oct 2025
- 25 Oct 2026Generic approved · 021883-00126 Nov 2025
- 25 Oct 2026Generic approved · 021883-00110 Nov 2025
- 25 Oct 2026Generic approved · 021883-00126 Feb 2026
- 25 Oct 2026Generic approved · 021883-0014 Jun 2026
Products covered · 1
| NDA · product | Form | Strength | Listed expiry |
|---|---|---|---|
| 021883 · 001 · RLD | powder, intravenous | EQ 500MG BASE/VIAL | 23 May 2028 |