United States · FDA National Drug Code directory

TRIPROLIDINE HYDROCHLORIDE

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
69367-253_2ef4d962-1c92-48e3-bf24-200a275b3d08
Product NDC
69367-253
Form
SYRUP
Composition / generic term
TRIPROLIDINE HYDROCHLORIDE
Labeler
Westminster Pharmaceuticals, LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20200309
Source listing expiry
20271231

Source-listed ingredients

  • TRIPROLIDINE HYDROCHLORIDE — .938 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER · 69367-253-30

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.

Browse United States records →