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Betamethasone Dipropionate

NDC 51672-1340, Betamethasone Dipropionate, lotion, augmented, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1340
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
LOTION, AUGMENTED
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077477
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1340 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BETAMETHASONE DIPROPIONATE.5 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
51672-1340-3516721340031 BOTTLE in 1 CARTON (51672-1340-3) / 30 mL in 1 BOTTLE
51672-1340-4516721340041 BOTTLE in 1 CARTON (51672-1340-4) / 60 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3b23a3c0-3306-4a2d-932d-25916d16dc68

  • NADAC price for package 51672134003

    GET /v1/drugs/nadac/51672134003

  • NADAC price for package 51672134004

    GET /v1/drugs/nadac/51672134004

Use it

Look up 51672-1340 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1340 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1340. 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.