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Naproxen Sodium and Diphenhydramine HCl

Naproxen Sodium and Diphenhydramine HCl · NAPROXEN SODIUM 220 mg/1; DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1 · Tablet, Film Coated · Oral · Granules India Ltd

NDC 62207-0814-38 · 37500 TABLET, FILM COATED in 1 POUCH · ANDA · View full market →

The short version

Only one company currently supplies this market — there is no backup if it stumbles.

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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
ANDA213663
TE code
Approval date
Sep 24, 2020
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 Naproxen Sodium and Diphenhydramine HCl (Tablet, Film Coated)

LabelerStrengthFirst seenLast seen
Granules India LtdNAPROXEN SODIUM 220 mg/1; DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1Aug 26, 2026Sep 2, 2026
Granules India LtdNAPROXEN SODIUM 25 mg/1; DIPHENHYDRAMINE HYDROCHLORIDE 220 mg/1Jul 22, 2026Aug 19, 2026
Granules India LtdDIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1; NAPROXEN SODIUM 220 mg/1Jul 15, 2026Jul 15, 2026

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

Cite this page

DrugDashboards, "Naproxen Sodium and Diphenhydramine HCl — NDC 62207-0814-38," retrieved September 3, 2026, https://drugdashboards.com/drug/62207081438.

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