SUAVECITO 5% Minoxidil Solution
NDC 74866-414, MINOXIDIL, liquid, from SUAVECITO, INC..
- Product NDC
- 74866-414
- Status
- Listed
- Labeler
- SUAVECITO, INC.
- Dosage form
- LIQUID
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA076239
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/74866-414 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MINOXIDIL50 mg/mL
Pharmacologic classes
Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 74866-414-01 | 74866041401 | 1 BOTTLE in 1 BOX (74866-414-01) / 60 mL in 1 BOTTLE |
| 74866-414-03 | 74866041403 | 3 BOTTLE in 1 BOX (74866-414-03) / 60 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 74866-414 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/74866-414 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 74866-414. 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.