Propranolol Hydrochloride 68071-3576
Product NDC
68071-3576- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 13, 1986
- Listing Expires
- December 31, 2026
- Application
- ANDA070177
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 40 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
120 TABLET in 1 BOTTLE, PLASTIC (68071-3576-1)