Minoxidil
NDC 59726-116, Minoxidil, aerosol, foam, from P & L Development, LLC.
- Product NDC
- 59726-116
- Status
- Listed
- Labeler
- P & L Development, LLC
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA208092
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59726-116 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MINOXIDIL50 mg/g
Pharmacologic classes
Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59726-116-60 | 59726011660 | 60 g in 1 CAN (59726-116-60) |
| 59726-116-65 | 59726011665 | 2 CAN in 1 PACKAGE (59726-116-65) / 60 g in 1 CAN |
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 59726-116 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59726-116 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59726-116. 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.