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Betamethasone dipropionate

NDC 51672-1390, Betamethasone dipropionate, spray, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1390
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SPRAY
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211722
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1390 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BETAMETHASONE DIPROPIONATE.5 mg/g

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
51672-1390-4516721390041 BOTTLE in 1 CARTON (51672-1390-4) / 60 g in 1 BOTTLE
51672-1390-8516721390081 BOTTLE in 1 CARTON (51672-1390-8) / 120 g in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc3dd2f7-38ad-4c4c-8602-29b33cc6af90

Use it

Look up 51672-1390 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1390 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1390. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.