ivermectin

Generic: ivermectin

Labeler: mayne pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name ivermectin
Generic Name ivermectin
Labeler mayne pharma inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

ivermectin 10 mg/g

Manufacturer
Mayne Pharma Inc.

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)
antiparasitic [epc] pediculicide [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68308701
Hyphenated Format 68308-701

Supplemental Identifiers

RxCUI
1598068
UNII
8883YP2R6D
NUI
N0000175484 N0000181811

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
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (68308-701-45) / 45 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

ivermectin (10 mg/g)

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"}