ivermectin
Generic: ivermectin
Labeler: mayne pharma inc.Drug Facts
Product Profile
Brand Name
ivermectin
Generic Name
ivermectin
Labeler
mayne pharma inc.
Dosage Form
CREAM
Routes
Active Ingredients
ivermectin 10 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68308-701
Product ID
68308-701_180415ea-bcf7-49ef-92f4-41d58324d752
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA206255
Listing Expiration
2026-12-31
Marketing Start
2024-01-08
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68308701
Hyphenated Format
68308-701
Supplemental Identifiers
RxCUI
UNII
NUI
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
NDA206255 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/g
Packaging
- 1 TUBE in 1 CARTON (68308-701-45) / 45 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": "180415ea-bcf7-49ef-92f4-41d58324d752", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["1598068"], "spl_set_id": ["39fbf2b3-cd2f-4e04-99c4-ca4390fae2bd"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Mayne Pharma Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68308-701-45) / 45 g in 1 TUBE", "package_ndc": "68308-701-45", "marketing_start_date": "20240108"}], "brand_name": "IVERMECTIN", "product_id": "68308-701_180415ea-bcf7-49ef-92f4-41d58324d752", "dosage_form": "CREAM", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "68308-701", "generic_name": "IVERMECTIN", "labeler_name": "Mayne Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IVERMECTIN", "active_ingredients": [{"name": "IVERMECTIN", "strength": "10 mg/g"}], "application_number": "NDA206255", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240108", "listing_expiration_date": "20261231"}