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 Identifiers#

Field, Values table
FieldValues
Unii81BK194Z5M
Rxcui199107

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

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