Pyrantel Pamoate

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: Pyrantel Pamoate
Generic name: PYRANTEL PAMOATE
Manufacturer: ProMex LLC
Product type: HUMAN OTC DRUG
SPL set ID: e68c503a-6f79-4f83-a6f3-c12a13fb06a0
SPL ID: 26fb5b42-2803-4e62-a944-b0b31ad5ba60
Version: 5
Effective date: 2024-12-18
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:53:04

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		M024	openfda.application_number
brand name		Pyrantel Pamoate	openfda.brand_name
generic name		PYRANTEL PAMOATE	openfda.generic_name
manufacturer name		ProMex LLC	openfda.manufacturer_name
ndc	package	58988-1770-1	openfda.package_ndc
ndc	product	58988-1770	openfda.product_ndc
ndc11	package	58988177001	derived:openfda.package_ndc
rxcui		199106	openfda.rxcui
spl id		26fb5b42-2803-4e62-a944-b0b31ad5ba60	id
spl set id		e68c503a-6f79-4f83-a6f3-c12a13fb06a0	set_id
unii		81BK194Z5M	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 *Abdominal cramps, nausea, vomiting, diarrhea, headache, or dizziness sometimes occurs after taking this drug. If any of these conditions persist, consult a doctor. *If you are pregnant or have liver disease, do not take this product unless directed by a doctor.

Reported adverse events (FAERS/openFDA)#

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