Propranolol Hydrochloride 71610-0339
Product NDC
71610-0339- Manufacturer
- Aphena Pharma Solutions - Tennessee, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 19, 1985
- Listing Expires
- December 31, 2026
- Application
- ANDA070213
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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)
45 TABLET in 1 BOTTLE, PLASTIC (71610-339-45)
90 TABLET in 1 BOTTLE, PLASTIC (71610-339-60)