Minoxidil 49884-0257
Product NDC
49884-0257- Manufacturer
- Endo Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 14, 1988
- Listing Expires
- December 31, 2026
- Application
- ANDA071839
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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(2)
100 TABLET in 1 BOTTLE (49884-257-01)
500 TABLET in 1 BOTTLE (49884-257-05)