ultravate

Generic: halobetasol propionate

Labeler: lacer pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ultravate
Generic Name halobetasol propionate
Labeler lacer pharma, llc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

halobetasol propionate .5 mg/g

Manufacturer
Lacer Pharma, LLC

Identifiers & Regulatory

Product NDC 73159-008
Product ID 73159-008_32225bd7-54bb-93da-e063-6394a90aadc5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA208183
Listing Expiration 2026-12-31
Marketing Start 2025-04-06

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73159008
Hyphenated Format 73159-008

Supplemental Identifiers

RxCUI
1789962 1790329
UNII
91A0K1TY3Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ultravate (source: ndc)
Generic Name halobetasol propionate (source: ndc)
Application Number NDA208183 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (73159-008-60) / 59 g in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

halobetasol propionate (.5 mg/g)

Linked Drug Pages (1)

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"}