Propranolol Hydrochloride 17856-8728
Product NDC
17856-8728- Manufacturer
- Atlantic Biologicals Corp.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 15, 1987
- Listing Expires
- December 31, 2026
- Application
- ANDA070979
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 20 mg/5mL |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUP