ultravate
Generic: halobetasol propionate
Labeler: lacer pharma, llcDrug Facts
Product Profile
Brand Name
ultravate
Generic Name
halobetasol propionate
Labeler
lacer pharma, llc
Dosage Form
LOTION
Routes
Active Ingredients
halobetasol propionate .5 mg/g
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73159008
Hyphenated Format
73159-008
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- .5 mg/g
Packaging
- 1 BOTTLE in 1 CARTON (73159-008-60) / 59 g in 1 BOTTLE
Packages (1)
Ingredients (1)
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"}