pyrantel pamoate
Generic: pyrantel pamoate
Labeler: promex llcDrug Facts
Product Profile
Brand Name
pyrantel pamoate
Generic Name
pyrantel pamoate
Labeler
promex llc
Dosage Form
SUSPENSION
Routes
Active Ingredients
pyrantel pamoate 144 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
58988-1770
Product ID
58988-1770_26fb5b42-2803-4e62-a944-b0b31ad5ba60
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M024
Listing Expiration
2026-12-31
Marketing Start
2002-09-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
589881770
Hyphenated Format
58988-1770
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
pyrantel pamoate (source: ndc)
Generic Name
pyrantel pamoate (source: ndc)
Application Number
M024 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 144 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (58988-1770-1) / 30 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26fb5b42-2803-4e62-a944-b0b31ad5ba60", "openfda": {"unii": ["81BK194Z5M"], "rxcui": ["199106"], "spl_set_id": ["e68c503a-6f79-4f83-a6f3-c12a13fb06a0"], "manufacturer_name": ["ProMex LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58988-1770-1) / 30 mL in 1 BOTTLE", "package_ndc": "58988-1770-1", "marketing_start_date": "20020927"}], "brand_name": "Pyrantel Pamoate", "product_id": "58988-1770_26fb5b42-2803-4e62-a944-b0b31ad5ba60", "dosage_form": "SUSPENSION", "product_ndc": "58988-1770", "generic_name": "Pyrantel Pamoate", "labeler_name": "ProMex LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pyrantel Pamoate", "active_ingredients": [{"name": "PYRANTEL PAMOATE", "strength": "144 mg/mL"}], "application_number": "M024", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20020927", "listing_expiration_date": "20261231"}