Propranolol Hydrochloride 51991-0819
Product NDC
51991-0819- Manufacturer
- Breckenridge Pharmaceutical, Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 11, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA078703
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 120 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-819-01)
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-819-05)