vrmx 500
Generic: pyrantel pamoate
Labeler: opmx llcDrug Facts
Product Profile
Brand Name
vrmx 500
Generic Name
pyrantel pamoate
Labeler
opmx llc
Dosage Form
TABLET
Routes
Active Ingredients
pyrantel pamoate 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69729-141
Product ID
69729-141_10c1a1dd-9165-2eec-e063-6294a90a3a38
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M024
Listing Expiration
2026-12-31
Marketing Start
2022-06-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69729141
Hyphenated Format
69729-141
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
vrmx 500 (source: ndc)
Generic Name
pyrantel pamoate (source: ndc)
Application Number
M024 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (69729-141-10) / 10 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "10c1a1dd-9165-2eec-e063-6294a90a3a38", "openfda": {"unii": ["81BK194Z5M"], "rxcui": ["199107"], "spl_set_id": ["e119cad8-9814-7d5a-e053-2995a90afde5"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69729-141-10) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "69729-141-10", "marketing_start_date": "20220610"}], "brand_name": "VRMX 500", "product_id": "69729-141_10c1a1dd-9165-2eec-e063-6294a90a3a38", "dosage_form": "TABLET", "product_ndc": "69729-141", "generic_name": "PYRANTEL PAMOATE", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VRMX 500", "active_ingredients": [{"name": "PYRANTEL PAMOATE", "strength": "180 mg/1"}], "application_number": "M024", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220610", "listing_expiration_date": "20261231"}