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: e68dd24a-93f8-4e2e-a698-d9ad9a7cebac
SPL ID: 590596c7-cde5-419a-b5d2-759b8d996fba
Version: 2
Effective date: 2018-01-02
Source export date: 2026-11-06
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:48:53

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		part357B	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	58988-1760-1	openfda.package_ndc
ndc	product	58988-1760	openfda.product_ndc
ndc11	package	58988176001	derived:openfda.package_ndc
rxcui		199107	openfda.rxcui
spl id		590596c7-cde5-419a-b5d2-759b8d996fba	id
spl set id		e68dd24a-93f8-4e2e-a698-d9ad9a7cebac	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 occur after taking this drug. If any of these conditions persist consult a doctor If you are pregnant or have liver disease, don't take this product unless directed by a doctor.

Reported adverse events (FAERS/openFDA)#

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