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Clotrimazole and Betamethasone Dipropionate

NDC 51672-1308, Clotrimazole and Betamethasone Dipropionate, lotion, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1308
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
LOTION
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076493
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1308 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CLOTRIMAZOLE10 mg/mL
  • BETAMETHASONE DIPROPIONATE.5 mg/mL

Pharmacologic classes

Azole Antifungal [EPC]; Azoles [CS]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
51672-1308-3516721308031 BOTTLE in 1 CARTON (51672-1308-3) / 30 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e4e9f244-4a85-4c0d-9917-93182c4a6e87

  • NADAC price for package 51672130803

    GET /v1/drugs/nadac/51672130803

Use it

Look up 51672-1308 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1308 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1308. 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.