stromectol

Generic: ivermectin

Labeler: merck sharp & dohme llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name stromectol
Generic Name ivermectin
Labeler merck sharp & dohme llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ivermectin 3 mg/1

Manufacturer
Merck Sharp & Dohme LLC

Identifiers & Regulatory

Product NDC 0006-0032
Product ID 0006-0032_200e22cc-3187-4a71-b8e1-73d90edab8bf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA050742
Listing Expiration 2026-12-31
Marketing Start 1996-11-22

Pharmacologic Class

Established (EPC)
antiparasitic [epc] pediculicide [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00060032
Hyphenated Format 0006-0032

Supplemental Identifiers

RxCUI
261314 311207
UNII
8883YP2R6D
NUI
N0000175484 N0000181811

Packaging Origin

Original Packager
true

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 stromectol (source: ndc)
Generic Name ivermectin (source: ndc)
Application Number NDA050742 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (0006-0032-01) / 10 TABLET in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (0006-0032-20) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

0006-0032-01 2 BLISTER PACK in 1 CARTON (0006-0032-01) / 10 TABLET in 1 BLISTER PACK 0006-0032-20 2 BLISTER PACK in 1 CARTON (0006-0032-20) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

ivermectin (3 mg/1)

Linked Drug Pages (1)

STROMECTOL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "200e22cc-3187-4a71-b8e1-73d90edab8bf", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["261314", "311207"], "spl_set_id": ["681888c9-af79-4b7d-ae80-c3f4f6f1effd"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Merck Sharp & Dohme LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0006-0032-01)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0006-0032-01", "marketing_start_date": "20240920"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0006-0032-20)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0006-0032-20", "marketing_start_date": "19961122"}], "brand_name": "STROMECTOL", "product_id": "0006-0032_200e22cc-3187-4a71-b8e1-73d90edab8bf", "dosage_form": "TABLET", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "0006-0032", "generic_name": "ivermectin", "labeler_name": "Merck Sharp & Dohme LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "STROMECTOL", "active_ingredients": [{"name": "IVERMECTIN", "strength": "3 mg/1"}], "application_number": "NDA050742", "marketing_category": "NDA", "marketing_start_date": "19961122", "listing_expiration_date": "20261231"}