Propranolol Hydrochloride 67046-1657
Product NDC
67046-1657- Manufacturer
- Coupler Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 4, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA078955
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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(1)
30 TABLET in 1 BLISTER PACK (67046-1657-3)