Adapalene
NDC 51672-2150, Adapalene, gel, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 51672-2150
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- GEL
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA215940
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2150 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ADAPALENE1 mg/g
Pharmacologic classes
Retinoid [EPC]; Retinoids [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51672-2150-1 | 51672215001 | 1 TUBE in 1 CARTON (51672-2150-1) / 15 g in 1 TUBE |
| 51672-2150-6 | 51672215006 | 1 TUBE in 1 CARTON (51672-2150-6) / 45 g in 1 TUBE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
NADAC price for package 51672215001
GET /v1/drugs/nadac/51672215001NADAC price for package 51672215006
GET /v1/drugs/nadac/51672215006
Use it
Look up 51672-2150 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2150 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51672-2150. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.