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Betamethasone Dipropionate

NDC 51672-1309, Betamethasone Dipropionate, gel, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1309
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076508
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1309 \
  -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
51672-1309-1516721309011 TUBE in 1 CARTON (51672-1309-1) / 15 g in 1 TUBE
51672-1309-3516721309031 TUBE in 1 CARTON (51672-1309-3) / 50 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e041ceb2-8bda-4703-b663-804e7b462e32

  • NADAC price for package 51672130901

    GET /v1/drugs/nadac/51672130901

  • NADAC price for package 51672130903

    GET /v1/drugs/nadac/51672130903

Use it

Look up 51672-1309 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1309 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1309. 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.