Propranolol Hydrochloride 50090-7101
Product NDC
50090-7101- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 3, 2021
- Listing Expires
- December 31, 2026
- 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)
100 TABLET in 1 BOTTLE (50090-7101-1)
90 TABLET in 1 BOTTLE (50090-7101-6)