Nitrofurantoin 16571-0888
Product NDC
16571-0888- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2024
- Listing Expires
- December 31, 2026
- Application
- NDA009175
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nitrofurantoin | 50 mg/5mL |
Drug Class
Nitrofuran Antibacterial [EPC]Nitrofuran Antibacterial [EPC]Nitrofurans [CS]
Packaging Options(1)
1 BOTTLE in 1 CARTON (16571-888-06) / 60 mL in 1 BOTTLE