Package 76420-619-20

Brand: ivermectin

Generic: ivermectin
NDC Package

Package Facts

Identity

Package NDC 76420-619-20
Digits Only 7642061920
Product NDC 76420-619
Description

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

Marketing

Marketing Status
Marketed Since 2023-10-05
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": "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"}