Midodrine Hydrochloride 81469-0141
Product NDC
81469-0141- Manufacturer
- First Nation Group, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 13, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA217271
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Midodrine Hydrochloride | 10 mg/1 |
Drug Class
Adrenergic alpha-Agonists [MoA]alpha-Adrenergic Agonist [EPC]
Packaging Options(1)
90 TABLET in 1 BOTTLE (81469-141-90)