5% Minoxidil Topical Solution
- Product NDC
- 71724-400
- 11-digit product format
- 717240400
- Labeler code
- 71724
- Product ID
- 71724-400_d61cee92-80ab-e041-e053-2a95a90af250
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- FLPHARMACEUTICALS LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-01-19
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 5 g/100mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71724-400-60 | 71724040060 | 1 BOTTLE in 1 CARTON (71724-400-60) > 60 mL in 1 BOTTLE | 1 bottle | 2022-01-19 | 0000-00-00 | No | No | Current |