Minoxidil Topical Solution 2% 51672-2152
Product NDC
51672-2152- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Solution
- Route
- Topical
- Product Type
- Human Otc Drug
- Marketing Start
- September 1, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA218175
Active Ingredients
| Ingredient | Strength |
|---|---|
| Minoxidil | 20 mg/mL |
Drug Class
Arteriolar Vasodilator [EPC]Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(2)
1 BOTTLE in 1 CARTON (51672-2152-4) / 60 mL in 1 BOTTLE
3 BOTTLE in 1 CARTON (51672-2152-9) / 60 mL in 1 BOTTLE