Minoxidil Topical Solution 2% 20 mg/mL
Minoxidil Topical Solution 2% · SOLUTION · SUN PHARMACEUTICAL INDUSTRIES, INC.
Minoxidil Topical Solution 2% is a solution containing minoxidil topical solution 2% at 20 mg/mL, taken topical. Manufactured by SUN PHARMACEUTICAL INDUSTRIES, INC..
Key Facts
- Brand Name
- Minoxidil Topical Solution 2%
- Generic Name
- Minoxidil Topical Solution 2%
- NDC Code (Product)
51672-2152- Manufacturer
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Strength
- 20 mg/mL
- Dosage Form
- SOLUTION
- Route
- TOPICAL
- Marketing Status
- Application #
- ANDA218175
- Drug Class
- Arteriolar Vasodilator [EPC]
- Marketing Start
- 09/01/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Minoxidil Topical Solution 2% used for?
Minoxidil Topical Solution 2% contains Minoxidil Topical Solution 2%. It is a solution taken topical. Consult your doctor for specific uses.
Is Minoxidil Topical Solution 2% a controlled substance?
Minoxidil Topical Solution 2% is not classified as a controlled substance by the DEA.
What is the generic name for Minoxidil Topical Solution 2%?
The generic name for Minoxidil Topical Solution 2% is Minoxidil Topical Solution 2%. There are no other listed brand versions of Minoxidil Topical Solution 2%.
What is the NDC code for Minoxidil Topical Solution 2% 20 mg/mL?
The NDC (National Drug Code) for Minoxidil Topical Solution 2% 20 mg/mL is 51672-2152, listed by SUN PHARMACEUTICAL INDUSTRIES, INC..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)