DrugDashboards

Benzphetamine Hydrochloride

Benzphetamine Hydrochloride · BENZPHETAMINE HYDROCHLORIDE 50 mg/1 · Tablet, Film Coated · Oral · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

NDC 23155-0952-01 · 100 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.

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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
ANDA202061
TE code
AA
Approval date
Jan 27, 2012
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 Benzphetamine Hydrochloride (Tablet, Film Coated)

LabelerStrengthFirst seenLast seen
Epic Pharma, LLCBENZPHETAMINE HYDROCHLORIDE 50 mg/1Jul 15, 2026Sep 2, 2026
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.BENZPHETAMINE HYDROCHLORIDE 50 mg/1Jul 15, 2026Sep 2, 2026

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

Cite this page

DrugDashboards, "Benzphetamine Hydrochloride — NDC 23155-0952-01," retrieved September 3, 2026, https://drugdashboards.com/drug/23155095201.

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