FDA.reportPublic FDA data

Pyrantel Pamoate

Product NDC
58988-1760
11-digit product format
589881760
Labeler code
58988
Product ID
58988-1760_590596c7-cde5-419a-b5d2-759b8d996fba
Type
HUMAN OTC DRUG
Nonproprietary name
Pyrantel Pamoate
Dosage form
TABLET
Route
ORAL
Labeler
ProMex LLC
Application
part357B
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2002-09-27
Substance
PYRANTEL PAMOATE
Active strength
180 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pyrantel Pamoate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PYRANTEL PAMOATE180 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
81BK194Z5MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
199107Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e68dd24a-93f8-4e2e-a698-d9ad9a7cebacAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58988-1760-1Pyrantel Pamoate2 in 1 CARTONTABLET22
58988-1760-1Pyrantel Pamoate10 in 1 BLISTER PACKTABLET102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58988-1760PYRANTEL PAMOATE TABLET [PROMEX LLC]2Current NDC, Legacy NDC, 2 package rows20180112_e68dd24a-93f8-4e2e-a698-d9ad9a7cebac.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pyrantel PamoatePYRANTEL PAMOATEProMex LLCe68dd24a-93f8-4e2e-a698-d9ad9a7cebac2018-01-02WarningsExact identifier
ndc (product): 58988-1760

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199107pyrantel pamoate 180 MG Oral TabletPSNe68dd24a-93f8-4e2e-a698-d9ad9a7cebac2
199107pyrantel 180 MG Oral TabletSCDe68dd24a-93f8-4e2e-a698-d9ad9a7cebac2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58988-1760-1589881760012 BLISTER PACK in 1 CARTON (58988-1760-1) / 10 TABLET in 1 BLISTER PACK2 blister pack2002-09-270000-00-00NoNoCurrent