ivermectin
Generic: ivermectin
Labeler: edenbridge pharmaceuticals llc.Drug Facts
Product Profile
Brand Name
ivermectin
Generic Name
ivermectin
Labeler
edenbridge pharmaceuticals llc.
Dosage Form
TABLET
Routes
Active Ingredients
ivermectin 3 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42799-806
Product ID
42799-806_46410c0e-07e7-7194-e063-6394a90a3997
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204154
Listing Expiration
2026-12-31
Marketing Start
2014-11-15
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42799806
Hyphenated Format
42799-806
Supplemental Identifiers
RxCUI
UNII
NUI
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
ivermectin (source: ndc)
Generic Name
ivermectin (source: ndc)
Application Number
ANDA204154 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (42799-806-01) / 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": "46410c0e-07e7-7194-e063-6394a90a3997", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["311207"], "spl_set_id": ["847a1dd7-d65b-4a0e-a67d-d90392059dac"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (42799-806-01) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "42799-806-01", "marketing_start_date": "20141115"}], "brand_name": "Ivermectin", "product_id": "42799-806_46410c0e-07e7-7194-e063-6394a90a3997", "dosage_form": "TABLET", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "42799-806", "generic_name": "Ivermectin", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ivermectin", "active_ingredients": [{"name": "IVERMECTIN", "strength": "3 mg/1"}], "application_number": "ANDA204154", "marketing_category": "ANDA", "marketing_start_date": "20141115", "listing_expiration_date": "20261231"}