ivermectin

Generic: ivermectin

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ivermectin
Generic Name ivermectin
Labeler asclemed usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ivermectin 3 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-619
Product ID 76420-619_06f2293c-2cf4-70d4-e063-6394a90a3a56
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)
antiparasitic [epc] pediculicide [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420619
Hyphenated Format 76420-619

Supplemental Identifiers

RxCUI
311207
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 ANDA204154 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (76420-619-20) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

76420-619-20 2 BLISTER PACK in 1 CARTON (76420-619-20) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

ivermectin (3 mg/1)

Linked Drug Pages (1)

Ivermectin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "06f2293c-2cf4-70d4-e063-6394a90a3a56", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["311207"], "spl_set_id": ["014e33e7-c07d-4feb-a2cf-7cd160b1facd"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (76420-619-20)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "76420-619-20", "marketing_start_date": "20231005"}], "brand_name": "Ivermectin", "product_id": "76420-619_06f2293c-2cf4-70d4-e063-6394a90a3a56", "dosage_form": "TABLET", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "76420-619", "generic_name": "Ivermectin", "labeler_name": "Asclemed USA, Inc.", "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"}