ivermectin
Generic: ivermectin
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
ivermectin
Generic Name
ivermectin
Labeler
sun pharmaceutical industries, inc.
Dosage Form
LOTION
Routes
Active Ingredients
ivermectin 5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51672-4230
Product ID
51672-4230_468c6f20-854b-ec91-e063-6394a90aeaa1
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA210720
Listing Expiration
2026-12-31
Marketing Start
2020-05-06
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516724230
Hyphenated Format
51672-4230
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
ANDA210720 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/g
Packaging
- 1 TUBE in 1 CARTON (51672-4230-8) / 117 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "468c6f20-854b-ec91-e063-6394a90aeaa1", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["1246673"], "spl_set_id": ["dd2c66e6-bd50-46df-a335-26215d02d13b"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-4230-8) / 117 g in 1 TUBE", "package_ndc": "51672-4230-8", "marketing_start_date": "20210106"}], "brand_name": "Ivermectin", "product_id": "51672-4230_468c6f20-854b-ec91-e063-6394a90aeaa1", "dosage_form": "LOTION", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "51672-4230", "generic_name": "Ivermectin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ivermectin", "active_ingredients": [{"name": "IVERMECTIN", "strength": "5 mg/g"}], "application_number": "ANDA210720", "marketing_category": "ANDA", "marketing_start_date": "20200506", "listing_expiration_date": "20261231"}