Propranolol Hydrochloride 51662-1338
Product NDC
51662-1338- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 22, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA077760
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 1 mg/mL |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
1 mL in 1 VIAL (51662-1338-1)
10 POUCH in 1 CASE (51662-1338-3) / 1 VIAL in 1 POUCH (51662-1338-2) / 1 mL in 1 VIAL