ULTRAVATE
NDC 73159-008, Halobetasol propionate, lotion, from Lacer Pharma, LLC.
- Product NDC
- 73159-008
- Status
- Listed
- Labeler
- Lacer Pharma, LLC
- Dosage form
- LOTION
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA208183
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/73159-008 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HALOBETASOL PROPIONATE.5 mg/g
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 73159-008-60 | 73159000860 | 1 BOTTLE in 1 CARTON (73159-008-60) / 59 g in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/74e899db-1c1f-48b2-9913-5d32a14906ae
Use it
Look up 73159-008 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/73159-008 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 73159-008. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.