Propranolol Hydrochloride 70518-4292
Product NDC
70518-4292- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 25, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA070322
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 40 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
30 TABLET in 1 BLISTER PACK (70518-4292-0)