Package 51672-4230-8

Brand: ivermectin

Generic: ivermectin
NDC Package

Package Facts

Identity

Package NDC 51672-4230-8
Digits Only 5167242308
Product NDC 51672-4230
Description

1 TUBE in 1 CARTON (51672-4230-8) / 117 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-01-06
Brand ivermectin
Generic ivermectin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "468c6f20-854b-ec91-e063-6394a90aeaa1", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["1246673"], "spl_set_id": ["dd2c66e6-bd50-46df-a335-26215d02d13b"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-4230-8)  / 117 g in 1 TUBE", "package_ndc": "51672-4230-8", "marketing_start_date": "20210106"}], "brand_name": "Ivermectin", "product_id": "51672-4230_468c6f20-854b-ec91-e063-6394a90aeaa1", "dosage_form": "LOTION", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "51672-4230", "generic_name": "Ivermectin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ivermectin", "active_ingredients": [{"name": "IVERMECTIN", "strength": "5 mg/g"}], "application_number": "ANDA210720", "marketing_category": "ANDA", "marketing_start_date": "20200506", "listing_expiration_date": "20261231"}