Package 73159-008-60

Brand: ultravate

Generic: halobetasol propionate
NDC Package

Package Facts

Identity

Package NDC 73159-008-60
Digits Only 7315900860
Product NDC 73159-008
Product ID 73159-008_32225bd7-54bb-93da-e063-6394a90aadc5
Description

1 BOTTLE in 1 CARTON (73159-008-60) / 59 g in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-04-06
Brand ultravate
Generic halobetasol propionate
Sample Package No

Linked Drug Pages (1)

ULTRAVATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "32225bd7-54bb-93da-e063-6394a90aadc5", "openfda": {"unii": ["91A0K1TY3Z"], "rxcui": ["1789962", "1790329"], "spl_set_id": ["74e899db-1c1f-48b2-9913-5d32a14906ae"], "manufacturer_name": ["Lacer Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (73159-008-60)  / 59 g in 1 BOTTLE", "package_ndc": "73159-008-60", "marketing_start_date": "20250406"}], "brand_name": "ULTRAVATE", "product_id": "73159-008_32225bd7-54bb-93da-e063-6394a90aadc5", "dosage_form": "LOTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "73159-008", "generic_name": "Halobetasol propionate", "labeler_name": "Lacer Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ULTRAVATE", "active_ingredients": [{"name": "HALOBETASOL PROPIONATE", "strength": ".5 mg/g"}], "application_number": "NDA208183", "marketing_category": "NDA", "marketing_start_date": "20250406", "listing_expiration_date": "20261231"}