Fluorouracil
NDC 51672-4062, Fluorouracil, solution, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 51672-4062
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076526
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4062 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUOROURACIL20 mg/mL
Pharmacologic classes
Nucleic Acid Synthesis Inhibitors [MoA]; Nucleoside Metabolic Inhibitor [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51672-4062-1 | 51672406201 | 1 BOTTLE in 1 CARTON (51672-4062-1) / 10 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1b2f6145-b338-42ed-88a7-f4da65c59164NADAC price for package 51672406201
GET /v1/drugs/nadac/51672406201
Use it
Look up 51672-4062 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4062 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51672-4062. 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.