Package 79903-154-01
Brand: ivermectin
Generic: ivermectinPackage Facts
Identity
Package NDC
79903-154-01
Digits Only
7990315401
Product NDC
79903-154
Description
1 TUBE in 1 CARTON (79903-154-01) / 117 g in 1 TUBE
Marketing
Marketing Status
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": "2b4be691-2fcd-a688-e063-6294a90a921b", "openfda": {"nui": ["N0000175484", "N0000181811"], "unii": ["8883YP2R6D"], "rxcui": ["1246673"], "spl_set_id": ["1608ec4a-2af4-4a43-a83f-5b25937068d1"], "pharm_class_epc": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (79903-154-01) / 117 g in 1 TUBE", "package_ndc": "79903-154-01", "marketing_start_date": "20221227"}], "brand_name": "Ivermectin", "product_id": "79903-154_2b4be691-2fcd-a688-e063-6294a90a921b", "dosage_form": "LOTION", "pharm_class": ["Antiparasitic [EPC]", "Pediculicide [EPC]"], "product_ndc": "79903-154", "generic_name": "Ivermectin", "labeler_name": "WALMART 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": "20221227", "listing_expiration_date": "20261231"}