Minoxidil 53489-0387
Product NDC
53489-0387- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 14, 1995
- Listing Expires
- December 31, 2027
- Application
- ANDA072709
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Minoxidil | 10 mg/1 |
Drug Class
Arteriolar Vasodilator [EPC]Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(4)
100 TABLET in 1 BOTTLE (53489-387-01)
250 TABLET in 1 BOTTLE (53489-387-03)
500 TABLET in 1 BOTTLE (53489-387-05)
1000 TABLET in 1 BOTTLE (53489-387-10)