ivermectin
Generic: ivermectin
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
ivermectin
Generic Name
ivermectin
Labeler
actavis pharma, inc.
Dosage Form
CREAM
Routes
Active Ingredients
ivermectin 10 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
0591-4052
Product ID
0591-4052_14ca838b-d540-4653-ac10-261e77906a51
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210019
Listing Expiration
2026-12-31
Marketing Start
2019-10-14
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05914052
Hyphenated Format
0591-4052
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
ANDA210019 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/g
Packaging
- 1 TUBE in 1 CARTON (0591-4052-89) / 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": "14ca838b-d540-4653-ac10-261e77906a51", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["1598068"], "spl_set_id": ["de9253c3-7d66-47fe-8ad7-8c0d4ee8ebda"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0591-4052-89) / 45 g in 1 TUBE", "package_ndc": "0591-4052-89", "marketing_start_date": "20191014"}], "brand_name": "Ivermectin", "product_id": "0591-4052_14ca838b-d540-4653-ac10-261e77906a51", "dosage_form": "CREAM", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "0591-4052", "generic_name": "Ivermectin", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ivermectin", "active_ingredients": [{"name": "IVERMECTIN", "strength": "10 mg/g"}], "application_number": "ANDA210019", "marketing_category": "ANDA", "marketing_start_date": "20191014", "listing_expiration_date": "20261231"}