Fluocinolone Acetonide
NDC 51672-1356, Fluocinolone Acetonide, oil, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 51672-1356
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- OIL
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202368
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1356 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUOCINOLONE ACETONIDE.11 mg/118.28mL
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51672-1356-8 | 51672135608 | 1 BOTTLE in 1 CARTON (51672-1356-8) / 118.28 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/22e9909a-47d2-4331-9b92-e7c4c2acf739NADAC price for package 51672135608
GET /v1/drugs/nadac/51672135608
Use it
Look up 51672-1356 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1356 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51672-1356. 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.