ivermectin

Generic: ivermectin

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ivermectin
Generic Name ivermectin
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ivermectin 3 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2242
Product ID 68071-2242_1d76541f-80d8-2a55-e063-6294a90aa5f9
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 680712242
Hyphenated Format 68071-2242

Supplemental Identifiers

RxCUI
311207
UPC
0368071224238
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 (68071-2242-3) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

ivermectin (3 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d76541f-80d8-2a55-e063-6294a90aa5f9", "openfda": {"nui": ["N0000175484", "N0000181811"], "upc": ["0368071224238"], "unii": ["8883YP2R6D"], "rxcui": ["311207"], "spl_set_id": ["ad6539f2-94de-1bc5-e053-2a95a90a4cf2"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (68071-2242-3)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "68071-2242-3", "marketing_start_date": "20141115"}], "brand_name": "Ivermectin", "product_id": "68071-2242_1d76541f-80d8-2a55-e063-6294a90aa5f9", "dosage_form": "TABLET", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "68071-2242", "generic_name": "Ivermectin", "labeler_name": "NuCare Pharmaceuticals,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"}