lombrix
Generic: pyrantel pamoate
Labeler: opmx llcDrug Facts
Product Profile
Brand Name
lombrix
Generic Name
pyrantel pamoate
Labeler
opmx llc
Dosage Form
TABLET
Routes
Active Ingredients
pyrantel pamoate 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69729-807
Product ID
69729-807_3f94048f-d2bd-5a1a-e063-6294a90adf52
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M024
Listing Expiration
2026-12-31
Marketing Start
2025-09-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69729807
Hyphenated Format
69729-807
Supplemental Identifiers
RxCUI
UPC
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
lombrix (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 (69729-807-10) / 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": "3f94048f-d2bd-5a1a-e063-6294a90adf52", "openfda": {"upc": ["0810053181768"], "unii": ["81BK194Z5M"], "rxcui": ["199107"], "spl_set_id": ["3f940481-8e75-0bc7-e063-6394a90af1cd"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69729-807-10) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "69729-807-10", "marketing_start_date": "20250924"}], "brand_name": "Lombrix", "product_id": "69729-807_3f94048f-d2bd-5a1a-e063-6294a90adf52", "dosage_form": "TABLET", "product_ndc": "69729-807", "generic_name": "PYRANTEL PAMOATE", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lombrix", "active_ingredients": [{"name": "PYRANTEL PAMOATE", "strength": "180 mg/1"}], "application_number": "M024", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250924", "listing_expiration_date": "20261231"}