United States · FDA National Drug Code directory

ZELAPAR

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0187-0453_ff911cbd-70ba-4034-8831-a81676d7811c
Product NDC
0187-0453
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
SELEGILINE HYDROCHLORIDE
Labeler
Bausch Health US, LLC
Marketing category
NDA
Marketing start / end (source format)
20060614 / 20280731

Source-listed ingredients

  • SELEGILINE HYDROCHLORIDE — 1.25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 POUCH in 1 CARTON (0187-0453-02) / 10 TABLET, ORALLY DISINTEGRATING in 1 POUCH · 0187-0453-02

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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