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ADAPALENE and BENZOYL PEROXIDE

NDC 51672-1364, ADAPALENE and BENZOYL PEROXIDE, gel, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1364
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206959
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1364 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ADAPALENE1 mg/g
  • BENZOYL PEROXIDE25 mg/g

Pharmacologic classes

Retinoid [EPC]; Retinoids [CS]

Package NDCNDC-11Package
51672-1364-3516721364031 BOTTLE, PUMP in 1 CARTON (51672-1364-3) / 45 g in 1 BOTTLE, PUMP
51672-1364-6516721364061 TUBE in 1 CARTON (51672-1364-6) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a53f1aa5-d3d1-45af-8728-8f36090f49da

  • NADAC price for package 51672136403

    GET /v1/drugs/nadac/51672136403

Use it

Look up 51672-1364 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1364 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1364. 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.