DrugDashboards

Rilpivirine

Rilpivirine · RILPIVIRINE HYDROCHLORIDE 25 mg/1 · Tablet, Film Coated · Oral · Laurus Labs Limited

NDC 42385-0999-30 · 30 TABLET, FILM COATED in 1 BOTTLE · ANDA · View full market →

The short version

Just 2 companies supply this market — thin enough that a single exit would be felt immediately.

The numbers behind every sentence are on this page below — and the Watch button emails you when any of them move.

Medicare Part D

No Medicare Part D plan in CMS's quarterly files lists this product. That usually means it is discontinued, a repackager's listing, or a product no plan has added to its formulary.

How Part D pricing works →

NADAC price per unit

No NADAC pricing on file for this NDC — NADAC covers drugs dispensed by retail community pharmacies.

Supply fragility

Not scored — fragility is computed for NADAC-priced NDCs.

Regulatory

Application
ANDA219788
TE code
AB
Approval date
Jul 10, 2026
Patents / exclusivity
None on file

Shortage history

No FDA shortage reports for this drug or its presentations.

Recalls (this NDC)

No enforcement reports list this package NDC.

Manufacturers of Rilpivirine (Tablet, Film Coated)

LabelerStrengthFirst seenLast seen
Somerset Therapeutics, LLCRILPIVIRINE HYDROCHLORIDE 25 mg/1Jul 15, 2026Sep 2, 2026
Laurus Labs LimitedRILPIVIRINE HYDROCHLORIDE 25 mg/1Jul 18, 2026Aug 29, 2026

Roster from daily NDC Directory diffs — first/last seen dates start July 2026.

Cite this page

DrugDashboards, "Rilpivirine — NDC 42385-0999-30," retrieved September 3, 2026, https://drugdashboards.com/drug/42385099930.

Free to cite with attribution — see how the data is put together.