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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
Request
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 NDCNDC-11Package
73159-008-60731590008601 BOTTLE in 1 CARTON (73159-008-60) / 59 g in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

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
curl https://api.healthcare.dev/v1/drugs/ndc/73159-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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.