TRIPROLIDINE HYDROCHLORIDE

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: TRIPROLIDINE HYDROCHLORIDE
Generic name: TRIPROLIDINE HYDROCHLORIDE
Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4eeffb6d-fc5e-48bc-95f6-ec4d5cb6e0d2
SPL ID: 2b55d682-834c-4b40-accc-1b564bbd94a5
Version: 1
Effective date: 2026-08-10
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:13:35

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		TRIPROLIDINE HYDROCHLORIDE	openfda.brand_name
generic name		TRIPROLIDINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Westminster Pharmaceuticals, LLC	openfda.manufacturer_name
ndc	package	69367-450-30	openfda.package_ndc
ndc	product	69367-450	openfda.product_ndc
ndc11	package	69367045030	derived:openfda.package_ndc
rxcui		1926926	openfda.rxcui
spl id		2b55d682-834c-4b40-accc-1b564bbd94a5	id
spl set id		4eeffb6d-fc5e-48bc-95f6-ec4d5cb6e0d2	set_id
unii		YAN7R5L890	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not exceed recommended dosage. Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland Ask a doctor before use if you are taking sedatives or tranquilizers When using this product may cause drowsiness excitability may occur, especially in children alcohol, sedatives and tranquilizers may increase the drowsiness effect avoid alcoholic beverages use caution when drivin a motor vehicle or operating machinery Stop use and ask a doctor if new symptoms occur Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.