United States · FDA National Drug Code directory
ULTRAVATE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 73159-008_32225bd7-54bb-93da-e063-6394a90aadc5
- Product NDC
- 73159-008
- Form
- LOTION
- Composition / generic term
- Halobetasol propionate
- Labeler
- Lacer Pharma, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20250406
- Source listing expiry
- 20261231
Source-listed ingredients
- HALOBETASOL PROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (73159-008-60) / 59 g in 1 BOTTLE · 73159-008-60
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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