Propranolol Hydrochloride 70518-3466
Product NDC
70518-3466- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 3, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA071972
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 20 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
30 TABLET in 1 BLISTER PACK (70518-3466-2)
30 TABLET in 1 BLISTER PACK (70518-3466-3)