Dehydrated Alcohol 51991-0999
Generic: Alcohol
Product NDC
51991-0999- Manufacturer
- Breckenridge Pharmaceutical Inc
- Dosage Form
- Injection, Solution
- Route
- Intra-Arterial
- Product Type
- Human Prescription Drug
- Marketing Start
- September 23, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA219444
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Alcohol | 1 mL/mL |
Packaging Options(1)
10 VIAL, GLASS in 1 CARTON (51991-999-17) / 5 mL in 1 VIAL, GLASS (51991-999-75)