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: Jefferson Labs
Product type: HUMAN OTC DRUG
SPL set ID: e862b337-2991-4b56-8584-fd80dccd725f
SPL ID: 7406132d-3c90-4bea-8a2d-c71873601f0c
Version: 16
Effective date: 2025-12-19
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:54:50

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 · 19 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		Jefferson Labs	openfda.manufacturer_name
ndc	package	51072-088-03	openfda.package_ndc
ndc	package	51072-088-00	openfda.package_ndc
ndc	package	51072-088-01	openfda.package_ndc
ndc	package	51072-088-02	openfda.package_ndc
ndc	package	51072-088-04	openfda.package_ndc
ndc	product	51072-088	openfda.product_ndc
ndc11	package	51072008803	derived:openfda.package_ndc
ndc11	package	51072008801	derived:openfda.package_ndc
ndc11	package	51072008802	derived:openfda.package_ndc
ndc11	package	51072008800	derived:openfda.package_ndc
ndc11	package	51072008804	derived:openfda.package_ndc
rxcui		312733	openfda.rxcui
spl id		7406132d-3c90-4bea-8a2d-c71873601f0c	id
spl set id		e862b337-2991-4b56-8584-fd80dccd725f	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 physician. Keep this and all medications out of reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. If you are pregnant or have liver disease, do not take this product unless directed by a physician.

Reported adverse events (FAERS/openFDA)#

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