Package 42799-806-01

Brand: ivermectin

Generic: ivermectin
NDC Package

Package Facts

Identity

Package NDC 42799-806-01
Digits Only 4279980601
Product NDC 42799-806
Description

2 BLISTER PACK in 1 CARTON (42799-806-01) / 10 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-11-15
Brand ivermectin
Generic ivermectin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46410c0e-07e7-7194-e063-6394a90a3997", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["311207"], "spl_set_id": ["847a1dd7-d65b-4a0e-a67d-d90392059dac"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (42799-806-01)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "42799-806-01", "marketing_start_date": "20141115"}], "brand_name": "Ivermectin", "product_id": "42799-806_46410c0e-07e7-7194-e063-6394a90a3997", "dosage_form": "TABLET", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "42799-806", "generic_name": "Ivermectin", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "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"}